| Primary Device ID | D8305605152 |
| NIH Device Record Key | a60f47cb-1017-4139-a73a-09cdcaff3a3f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Tyvek Self-Seal Pouch |
| Version Model Number | 560515 |
| Company DUNS | 246113039 |
| Company Name | GS Medical Packaging Inc |
| Device Count | 200 |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | D8305605150 [Unit of Use] |
| HIBCC | D8305605151 [Primary] |
| HIBCC | D8305605152 [Package] Contains: D8305605151 Package: Cardboard Box [5 Units] In Commercial Distribution |
| FRG | Wrap, Sterilization |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-01-10 |
| Device Publish Date | 2025-01-02 |
| D8305610152 | Tyvek 10” x 15” Self-Seal Pouch |
| D8305608162 | Tyvek 8” x 16” Self-Seal Pouch |
| D8305607132 | Tyvek 7” x 13” Self-Seal Pouch |
| D8305606132 | Tyvek 6” x 12.5” Self-Seal Pouch |
| D8305605152 | Tyvek 5” x 15” Self-Seal Pouch |
| D8305604092 | Tyvek 3.5” x 9” Self-Seal pouch |