| Primary Device ID | 50707387767261 |
| NIH Device Record Key | 0f73fc92-a30c-4a12-bbb3-b31a2955ec5b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Steri-Vac™ |
| Version Model Number | GS8-1D |
| Catalog Number | GS8-1D |
| Company DUNS | 830016148 |
| Company Name | 3M COMPANY |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Phone | +1(800)228-3957 |
| 3Mhealthcarecompliance@mmm.com | |
| Phone | +1(800)228-3957 |
| 3Mhealthcarecompliance@mmm.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 50707387767261 [Primary] |
| FLF | Sterilizer, ethylene-oxide gas |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-24 |
| 50707387767278 | 3M™ Steri-Vac™ Sterilizer, 2 Door GS8-2D |
| 50707387767261 | 3M™ Steri-Vac™ Sterilizer, 1 Door GS8-1D |
| 50707387767254 | 3M™ Steri-Vac™ Sterilizer, 2 Door GS5-2D |
| 50707387767247 | 3M™ Steri-Vac™ Sterilizer, 1 Door GS5-1D |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() STERI-VAC 72203060 0790797 Live/Registered |
ADVANCED PRODUCTS CORP. 1964-10-01 |
![]() STERI-VAC 72078851 0728896 Dead/Cancelled |
Chili Products Corporation Ltd. 1959-08-03 |