Primary Device ID | 00840117343375 |
NIH Device Record Key | adc60f10-94e3-47ab-b4af-c6dda21b4ae7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Durma+ Collagen Wound Dressing, 7" x 7" |
Version Model Number | 3099 |
Company DUNS | 008124539 |
Company Name | Dynarex Corporation |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840117343290 [Package] Contains: 00840117343337 Package: Case [10 Units] In Commercial Distribution |
GS1 | 00840117343337 [Package] Package: Box [5 Units] In Commercial Distribution |
GS1 | 00840117343375 [Primary] |
KGN | Wound Dressing With Animal-Derived Material(S) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-06-11 |
Device Publish Date | 2025-06-03 |