Primary Device ID | 08717903492918 |
NIH Device Record Key | 34666560-bd35-4b7f-85f4-e94dcf2523b7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Micrograft gauze + cork plate, 1:9 |
Version Model Number | 2.9/1 |
Catalog Number | 2.9/1 |
Company DUNS | 489831498 |
Company Name | Humeca B.V. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | 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 | 08717903490075 [Primary] |
GS1 | 08717903492918 [Package] Contains: 08717903490075 Package: Box [10 Units] In Commercial Distribution |
GS1 | 08717903492949 [Package] Contains: 08717903490075 Package: Box [40 Units] In Commercial Distribution |
GFD | Dermatome |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-05-27 |
Device Publish Date | 2025-05-19 |