DermaFilm Thin With border

GUDID 00714196391803

DERMARITE INDUSTRIES LLC

Exudate-absorbent dressing, non-gel, non-antimicrobial
Primary Device ID00714196391803
NIH Device Record Key03b7b102-6b49-4f5b-b2ec-728a023d1c99
Commercial Distribution StatusIn Commercial Distribution
Brand NameDermaFilm Thin With border
Version Model Number32670
Company DUNS883925562
Company NameDERMARITE INDUSTRIES LLC
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100714196391803 [Primary]

FDA Product Code

NADDressing, Wound, Occlusive

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-09-17
Device Publish Date2021-09-09

On-Brand Devices [DermaFilm Thin With border]

0071419632670632670
0071419630666100306E
0071419625944800259E
0071419622922900229E
0071419639180332670
0071419639176600306E
0071419639174200259E
0071419639178000229E

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.