Primary Device ID | 00714196114105 |
NIH Device Record Key | e336f713-ae3a-432f-9c70-730b54ae50d3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sterile Bordered Gauze |
Version Model Number | 11410 |
Company DUNS | 883925562 |
Company Name | DERMARITE INDUSTRIES LLC |
Device Count | 25 |
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 | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00714196114105 [Primary] |
GS1 | 01714196114104 [Unit of Use] |
NAC | Dressing, Wound, Hydrophilic |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-09-09 |
Device Publish Date | 2020-09-01 |
00714196263667 | 00263E |
00714196262448 | 00262E |
00714196261229 | 00261E |
00714196114808 | 11480 |
00714196114501 | 11450 |
00714196114143 | 11414 |
00714196114105 | 11410 |
00714196113641 | 11364 |
00714196112309 | 11230 |
00714196390448 | 00263E |
00714196390424 | 00262E |
00714196390400 | 00261E |
00714196390387 | 11480 |
00714196390363 | 11450 |
00714196390349 | 11414 |
00714196390325 | 11410 |
00714196390301 | 11364 |
00714196390288 | 11230 |