Primary Device ID | 00714196251459 |
NIH Device Record Key | f4458b27-4b91-4882-a722-8a97395b5b5b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DermaView |
Version Model Number | 00251E |
Company DUNS | 883925562 |
Company Name | DERMARITE INDUSTRIES LLC |
Device Count | 50 |
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 | 00714196251459 [Primary] |
GS1 | 01714196251458 [Unit of Use] |
KMK | Device, Intravascular Catheter Securement |
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 |
00714196251459 | 00251E |
00714196241238 | 00241E |
00714196392381 | 00251E |
00714196392343 | 00241E |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() DERMAVIEW 78045361 not registered Dead/Abandoned |
George Medical, LLC 2001-01-29 |
![]() DERMAVIEW 74175207 1866584 Dead/Cancelled |
ARAMIS INC. 1991-06-11 |
![]() DERMAVIEW 74175205 1833138 Dead/Cancelled |
ARAMIS INC. 1991-06-11 |