Primary Device ID | D830442101BULK2 |
NIH Device Record Key | 7e6da32c-0277-41c6-aaf6-4f8befab4d70 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PROFESSIONAL'S CHOICE |
Version Model Number | 442101BULK |
Company DUNS | 246113039 |
Company Name | GS Medical Packaging Inc |
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 | 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 | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | 9052711523 |
accounting@gsmedicalpackaging.com | |
Phone | 9052711523 |
accounting@gsmedicalpackaging.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | D830442101BULK1 [Package] Contains: D830442101BULK9 Package: CARDBOARD BOX [200 Units] In Commercial Distribution |
HIBCC | D830442101BULK2 [Package] Contains: D830442101BULK1 Package: CARDBOARD BOX [30 Units] In Commercial Distribution |
HIBCC | D830442101BULK9 [Primary] |
KCT | Sterilization Wrap Containers, Trays, Cassettes & Other Accessories |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2017-02-07 |