Primary Device ID | 00714196390868 |
NIH Device Record Key | a0817401-ad7e-4a4f-9ea4-3ab0a92d3e6c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ComfortFoam Border |
Version Model Number | 43680 |
Company DUNS | 883925562 |
Company Name | DERMARITE INDUSTRIES LLC |
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 | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00714196390868 [Primary] |
NAD | Dressing, Wound, Occlusive |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-09-17 |
Device Publish Date | 2021-09-09 |
00714196437709 | 43770 |
00714196436801 | 43680 |
00714196434807 | 43480 |
00714196434128 | 43412 |
00714196433305 | 43330 |
00714196432506 | 43250 |
00714196432209 | 43220 |
00714196318664 | 00318E |
00714196317445 | 00317E |
00714196390882 | 43770 |
00714196390868 | 43680 |
00714196390844 | 43480 |
00714196390820 | 43412 |
00714196390806 | 43330 |
00714196390783 | 43250 |
00714196390769 | 43220 |
00714196390745 | 00318E |
00714196390721 | 00317E |