Certifications: Table of Contents Document # Title Page(s) 1 ISO 17025: Certificate of Accreditation 2 2 ISO 17025: Scope of Accreditation 3-7 3 FDA: Medical Device Establishment 8 Registration 4 FDA: Generic Drug Statement of 9 Compliance 5 FDA: Drug Establishments Registration 10 6 FDA: Establishment Registration and 11 Listing for Human Cells, Tissues, and Cellular and Tissue-Based Products (HCT/Ps) 7 EU/EMA: European Certificate of GMP 12-13 Compliance 8 TGA: Certificate of GMP Compliance 14-15 9 US: DEA Registration 16 10 Utah: State Business License 17 6280 S. Redwood Road, Salt Lake City, UT, 84123 801-290-7500 nelsonlabs.com
CERTIFICATE OF ACCREDITATION ANSI-ASQ National Accreditation Board 500 Montgomery Street, Suite 625, Alexandria, VA 22314, 877-344-3044 This is to certify that Nelson Laboratories, LLC 6280 S. Redwood Road Salt Lake City, UT 84123 has been assessed by ANAB and meets the requirements of international standard ISO/IEC 17025:2005 while demonstrating technical competence in the field of TESTING Refer to the accompanying Scope of Accreditation for information regarding the types of tests to which this accreditation applies. AT-1382 Certificate Number Certificate Valid: 03/01/2018-03/16/2019 Version No. 004 Issued: 03/01/2018 This laboratory is accredited in accordance with the recognized International Standard ISO/IEC 17025:2005. This accreditation demonstrates technical competence for a defined scope and the operation of a laboratory quality management system (refer to joint ISO-ILAC-IAF Communiqué dated April 2017).
SCOPE OF ACCREDITATION TO ISO/IEC 17025:2005 Nelson Laboratories, LLC 6280 S. Redwood Road, Salt Lake City, UT 84123 Kevin Buckingham 801-290-7500 KBuckingham@nelsonlabs.com www.nelsonlabs.com TESTING Valid to: March 16, 2019 Certificate Number: AT-1382 Microbiological Specific Tests and/or Properties Measured Agar Overlay Antimicrobial Preservative Effectiveness Bacterial Endotoxins Bacterial Filtration Efficiency (BFE) Viral Filtration Efficiency (VFE) Barrier Testing (Viral Penetration) Bioburden Specification, Standard, Method, or Test Technique STP0031 based on ANSI/AAMI/ISO 10993-1,5,12 USP <87>, USP<1031> STP0131 based on USP <51>, STP0132 based on USP <51> and EP 5.1.3 STP0046 based on USP <85>, USP<161>, USP<797>, AAMI ST72, EP 2.6.14, ASTM D7102-04, BS EN 455-3 STP00004 and STP0007 based on ASTM F2101, EN14683, ASTM F2100 STP0062 and STP0174 based on ASTM F1671, AAMI PB70, ISO16604 STP0036 based on ISO 11737-1, STP0050 based on ISO11737-2, 11137-01 and -02, AAMI TIR 17, 35, 37, STP0051 based on ISO 11737-01 and -02, 11137-01 and -02, AAMI TIR 17, 33, 37 and STP0044 based on ISO11137-01 and -02, AAMI TIR 33, 35 Items, Materials or Product Tested Medical Devices, Raw Materials Antimicrobial Preservatives Medical Devices, Drugs Medical & Surgical Face Masks Textiles, Gloves Textiles, Medical Devices, Tissues, Pharmaceuticals Key Equipment or Technology ISO Class 5 Hoods Microscope Microplate Reader Andersen Sampler ISO Class 5 Hoods ISO Class 5 Hoods Version 004 Issued: March 1, 2018 www.anab.org Page 1 of 5
Microbiological Specific Tests and/or Properties Measured Biological Indicators (Population verification, Process Challenge Device (PCD) Preparation, BI Sterility) Cleaning, Disinfection, Sterilization Including the following subanalyses (separately accredited): Hemoglobin Protein Carbohydrates MEM elution TOC Bioburden Container Closure (Bacterial Ingress) Hemolysis MEM Elution Microbial Retention (Including Filter Bubble Point/Integrity Test) Specification, Standard, Items, Materials or Method, or Test Technique Product Tested STP0045, STP0079, and SOP0180 based on USP<55>, ISO 11138-1 to -4, ISO 11135-1 to -2, ISO 14161, BIs, PCDs ISO 14937, ISO 17665-2, AAMI TIR 13, 14, 16, BS EN 550 STP0083and STP0129 based on AAMI TIR 12, 30, ASTM E1837, ISO17664 STP0086 based on ANSI/AAMI ST79, AAMITIR12, ANSI/AAMI/ISO 17665, USP <1211> STP0152 based on AAMI TIR 12, USP<1211>, ANSI/AAMI/ ISO 11135-1 STP0153 based on ANSI/AAMI/ISO 14937, AAMI TIR12, USP <1211> STP0159 based on ISO 17664, ANSI/AAMI ST79, ANSI/AAMI ST77, ANSI/AAMI/ISO 11135, AAMI TIR30 STP0164 based on PDA TR 27 and FDA Guidance for Industry: Container and Closure Integrity Testing STP0093 based on ANSI/AAMI/ISO 10993-1,4,12 and ASTM F756-08 STP0032 based on ANSI/AAMI/ ISO 10993-1,5,12 USP <87>, USP<1031> STP0103 based on ASTM F838-15 Medical Devices, Reusable Devices Packaging Materials for Medical Device & Pharmaceutical Medical Devices, Raw Materials Medical Devices, Raw Materials Filters Key Equipment or Technology BI Sterility Suite ISO Class 5 Hoods Incubator Washer/Disinfectors Sterilizers (Steam, EO, VHP) UV/VIS Spectrophotometer Pressure/Vacuum Vessel Spectrophotometer ISO Class 5 Hoods Microscope Flow Meter Pressure Gauge ISO Class 5 Hood Version 004 Issued: March 1, 2018 www.anab.org Page 2 of 5
Microbiological Specific Tests and/or Properties Measured Microbiological Examination of NonSterile Products (Enumeration and Specified Organisms, USP 61/62) Organism Identification (Genetic and Gram Stain) Product Sterility & Bacteriostasis /Fungistasis (B/F) Standard Plate Counts Specification, Standard, Method, or Test Technique STP0169 and STP0165 based on USP<61> and USP<62> STP0105, STP0173 and STP0037 based on USP<1113> STP0077 and STP0078 based on USP<71>, USP<161>, USP<797>, ISO 11737-2, 1137-01 and -02, PIC/S PI 012-3, EP 2.6.1, JP V 4.06, ISO 17665, AAMI TIR 33 STP-0035 based on USP <71> STP0169 based on USP<61> Items, Materials or Product Tested Medical Devices, Pharmaceuticals Medical Devices, Pharmaceuticals Medical Devices, Pharmaceuticals, Biologics, Tissues Water, Food, Cosmetics, Pharmaceuticals Key Equipment or Technology ISO Class 5 Hoods Genetic Sequencers Thermocyclers Automatic Gram Stainer ISO Class 5 Hoods Microscopes ISO Class 5 Cleanrooms and Hoods ISO Class 5 Hoods Physical/ Chemical Testing Specific Tests and/or Properties Measured Barrier Testing: Synthetic Blood and Water Resistance (Hydrostatic Pressure, Impact Penetration) Container Closure (Dye Ingress) Ethylene Oxide (EO) Residual Analysis Specification, Standard, Method, or Test Technique STP0061, STP0071 and STP0072 based on ASTM F1670, AAMI PB70, ISO 16603, AATCC 42 and 127 STP0149 based on ANSI/AAMI/ISO 11607-1,2, ASTM D4491-07, PDA TR 27and FDA Guidance for Industry: Container and Closure Integrity Testing STP0016 based on ANSI/AMMI/ISO10993-7, 2008, USP <621> Items, Materials or Product Tested Textiles, Gloves Packaging Materials for Medical Device & Pharmaceutical Medical Devices Key Equipment or Technology Textiles, Gloves Packaging Materials for Medical Device & Pharmaceutical Medical Devices Version 004 Issued: March 1, 2018 www.anab.org Page 3 of 5
Physical/ Chemical Testing Specific Tests and/or Properties Measured FTIR, Material Characterization Particulates Particulate Filtration Efficiency (PFE) Respirator Certification Testing (NIOSH N95/N99) Respirator Inhalation/Exhalation Respirator Valve Leak Sodium Chloride Aerosol Test Water Purity Analysis TOC Conductivity ph Biological Marker Analysis Hemoglobin Protein Carbohydrates Specification, Standard, Items, Materials or Method, or Test Technique Product Tested STP0021 based on Polymers, Non-volatile USP<851>and USP<197> Residue, Materials STP0011 based on USP <788>, <789>, EP Medical Devices, Injectables 2.9.19, 2.9.31, BP Appendix and Ophthalmic Solutions, III A, Pharmaceutical Products BH EN 45502-1, 45502-2-1 ISO 8536-4 STP0005 based on ASTM Medical & Surgical Face F2299 Masks STP 145 based on 42 CFR Part 84 and NIOSH TEB APR-STP-007, RCT- APR- STP-003 STP0143 based on 42 CFR Part 84 and NIOSH TEB- Respirators APR-STP-0004 STP0014 based on 42 CFR Part 84and NIOSH TEB- ARP-STP-0058, TEB-ARP- STP-0059 STP0024 and STP0099 based on USP<1231>, USP<1230> and all USP monograph waters, Water USP, STP0028 based on Water EP USP<643> STP0029 based on USP<791> STP0147 based on USP<645> STP0087, STP0088, STP0089, and STP0183 based on ASTM F756-13, AAMI Medical Devices, Reusable TIR30, and Cleaning, Devices Disinfection, Sterilization references previously listed. Key Equipment or Technology Polymers, Non-volatile Residue, Materials Medical Devices, Injectables and Ophthalmic Solutions, Pharmaceutical Products Medical & Surgical Face Masks Respirators Water USP, Water EP Medical Devices, Reusable Devices Version 004 Issued: March 1, 2018 www.anab.org Page 4 of 5
Microbiological and Physical/ Chemical Testing Specific Tests and/or Properties Measured EN 13795: Performance requirements for surgical gowns and drapes Microbial penetration resistance Microbial evaluation (bioburden) Particle evaluation Liquid penetration resistance Burst strength Tensile Strength Note: Specification, Standard, Method, or Test Technique STP191 based on EN ISO22610 and EN ISO 22612 STP0036 based on ISO 11737-1 (Bioburden method) STP0144 based on EN ISO 9073-10 STP0071 based on AATCC 127 and EN 20811 STP0192 based on EN ISO 13938-1 STP0066 EN 29073-3 Items, Materials or Product Tested Medical & Surgical Gowns and Drapes 1. This scope is formatted as part of a single document including Certificate of Accreditation No. AT-1382. Key Equipment or Technology ISO Class 5 Hoods Gelbo Flex Unit Particle counter Burst tester Instron (Tensile) tester Version 004 Issued: March 1, 2018 www.anab.org Page 5 of 5
Virgil M. McCarthy From: CDRH Registration and Listing [mailto:reglist@cdrh.fda.gov] Sent: Saturday, October 07, 2017 7:39 PM To: DeMent, Aaron Subject: Registration Number 1721109: Successful 2018 Medical Device Establishment Registration Dear Aaron DeMent: This e-mail provides confirmation that the annual registration for the following medical device establishment has been successfully completed for 2018: Registration Number: 1721109 Owner Operator Number: 10029425 NELSON LABORATORIES, LLC 6280 S Redwood Rd Salt Lake City, UT 84123 UNITED STATES If you do not see a registration number assigned to the establishment and your establishment previously had one, please send an email to reglist@cdrh.fda.gov and include the registration number you believe is assigned to your establishment. We will review and determine if a duplicate registration has been created for your establishment. Your registration is valid until December 31, 2018. Registration for 2019 will be conducted between October 1 and December 31, 2018. Please note that registering your device facility and listing your devices does not, in any way, constitute FDA approval of your facility or your devices. Should you have any questions, please send an e-mail to the CDRH Registration and Listing Helpdesk at reglist@cdrh.fda.gov. CDRH Registration and Listing Helpdesk Office of Compliance Center for Devices and Radiological Health U.S. Food and Drug Administration Tel: 301-796-7400, Option 1 Email: reglist@cdrh.fda.gov 09 Oct 2017 12:57 PM
12. HCT/Ps REGULATED AS MEDICAL DEVICES 11. HCT/Ps DESCRIBED IN 21 CFR 1271.10 DEPARTMENT OF HEALTH AND HUMAN SERVICES PUBLIC HEALTH SERVICE FOOD AND DRUG ADMINISTRATION ESTABLISHMENT REGISTRATION AND LISTING FOR HUMAN CELLS, TISSUES, AND CELLULAR AND TISSUE-BASED PRODUCTS (HCT/Ps) (See reverse side for instructions) PART I - ESTABLISHMENT INFORMATION 3. OTHER FDA REGISTRATIONS a. BLOOD FDA 2830 b. DEVICES FDA 2891 NO. NO. FEI: 0001721109 FEI: 3000233845 d. INACTIVE PART II - PRODUCT INFORMATION 10. ESTABLISHMENT FUNCTIONS AND TYPES OF HCT / Ps Establishment Functions Types of HCT / Ps See Instructions for OMB Statement. FORM APPROVED:OMB No.0910-0543. Expiration Date: 6/30/2020 1. REGISTRATION NUMBER 2. REASON FOR SUBMISSION (FDA Establishment Identifier) a. INITIAL REGISTRATION / LISTING b. ANNUAL REGISTRATION / LISTING c. CHANGE IN INFORMATION Recover Screen Test Package Process Store Label Distribute VALIDATION--FOR FDA USE ONLY VALIDATED BY FDA:20-NOV-2017 DISTRICT: Denver PRINTED BY FDA:27-JAN-2018 13. HCT/Ps REGULATED AS DRUGS OR BIOLOGICAL DRUGS 14. PROPRIETARY NAME(S) 1 c. DRUG FDA 2656 NO. FEI: 0151663234 4. PHYSICAL LOCATION (Include legal name, number and street, city, state, country, and post office code) Nelson Laboratories, LLC a. Bone b. Cartilage 6280 South Redwood Road Salt Lake City, Utah 84123 c. Cornea d. Dura Mater a. PHONE 801-290-7500 ET b. SATELLITE RECOVERY ESTABLISHMENT (MANUFACTURING ESTABLISHMENT FEI NO. c. TESTING FOR MICRO-ORGANISMS ONLY 5. ENTER CORRECTIONS TO ITEM 4 e. Embryo f. Fascia g. Heart Valve h. Ligament SIP Directed Anonymous 6. MAILING ADDRESS OF REPORTING OFFICIAL (Include institution name if applicable, number and street, city, state, country, and post office code) Nelson Laboratories, LLC Attn: Matthew D. Cushing, BS 6280 South Redwood Road Salt Lake City, Utah 84123 i. Oocyte j. Pericardium k. Peripheral Blood Stem SIP Directed Anonymous Autologous Family Related Allogeneic l. Sclera a. PHONE 801-290-7692 ET 7. ENTER CORRECTIONS TO ITEM 6 b. PHONE m. Semen n. Skin SIP Directed Anonymous o. Somatic Cell Therapy Products Autologous Family Related Allogeneic 8. U.S. AGENT p. Tendon a. E-MAIL 9. REPORTING OFFICIAL'S SIGNATURE a. TYPED NAME Matthew D. Cushing, BS b. E-MAIL MCushing@nelsonlabs.com c. TITLE Director of Regulatory Affairs FORM FDA - 3356 (7/17) d. DATE 20-NOV-2017 q. Umbilical Cord Blood r. Vascular Graft s. t. u. v. Autologous Family Related Allogeneic
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RN0504274 1,2,2N 3,3N,4,5 10-31-2018 ANALYTICAL LAB $244.00 09-07-2017 NELSON LABORATORIES, LLC 6280 SOUTH REDWOOD RD SALT LAKE CITY, UT 84123 RN0504274 1,2,2N 3,3N,4,5 10-31-2018 ANALYTICAL LAB NELSON LABORATORIES, LLC 6280 SOUTH REDWOOD RD SALT LAKE CITY, UT 84123 $244.00 09-07-2017