Primary Device ID | 10818087012796 |
NIH Device Record Key | 7d88493b-ce82-4d57-afc7-b89f4d17befd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Propper Steri-Wrap® Unite™ 48" x 48" Sterilization Wrap |
Version Model Number | 31504800 |
Catalog Number | 31504800 |
Company DUNS | 001483130 |
Company Name | PROPPER MANUFACTURING COMPANY, INC. |
Device Count | 48 |
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 | true |
Manufacturing Date | false |
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 |
---|---|
GS1 | 10818087012796 [Unit of Use] |
GS1 | 70818087012798 [Primary] |
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 | 2021-09-13 |
Device Publish Date | 2021-09-03 |
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