Primary Device ID | D8304420892 |
NIH Device Record Key | f80af29d-3f6f-4fde-83e9-27219cbd1c1b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PROFESSIONAL'S CHOICE |
Version Model Number | 442089 |
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 |
Device Issuing Agency | Device ID |
---|---|
HIBCC | D830442089 [Primary] |
HIBCC | D8304420891 [Package] Contains: D830442089 Package: CARDBOARD BOX [200 Units] In Commercial Distribution |
HIBCC | D8304420892 [Package] Contains: D8304420891 Package: CARDBOARD BOX [12 Units] In Commercial Distribution |
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 | 2016-10-06 |