Primary Device ID | D8305610152 |
NIH Device Record Key | a6e68e02-272f-4ec7-a2b6-af1ade5ec348 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tyvek Self-Seal Pouch |
Version Model Number | 561015 |
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 | D8305610150 [Unit of Use] |
HIBCC | D8305610151 [Primary] |
HIBCC | D8305610152 [Package] Contains: D8305610151 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 |