DermaFilm X-Thin Clear with Grid

GUDID 00714196391681

DERMARITE INDUSTRIES LLC

Exudate-absorbent dressing, non-gel, non-antimicrobial Exudate-absorbent dressing, non-gel, non-antimicrobial Exudate-absorbent dressing, non-gel, non-antimicrobial Exudate-absorbent dressing, non-gel, non-antimicrobial Exudate-absorbent dressing, non-gel, non-antimicrobial Exudate-absorbent dressing, non-gel, non-antimicrobial Exudate-absorbent dressing, non-gel, non-antimicrobial Exudate-absorbent dressing, non-gel, non-antimicrobial Exudate-absorbent dressing, non-gel, non-antimicrobial

Primary Device ID	00714196391681
NIH Device Record Key	273e19e8-9c41-49d5-b9d4-651762d14839
Commercial Distribution Status	In Commercial Distribution
Brand Name	DermaFilm X-Thin Clear with Grid
Version Model Number	31460
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 Identifiers

Device Issuing Agency	Device ID
GS1	00714196391681 [Primary]

FDA Product Code

NAD	Dressing, Wound, Occlusive

Sterilization

Steralize Prior To Use	false
Device Is Sterile	true

Device Entry Metadata

Public Version Status	New
Device Record Status	Published
Public Version Number	1
Public Version Date	2021-09-17
Device Publish Date	2021-09-09

On-Brand Devices [DermaFilm X-Thin Clear with Grid ]

00714196314604	31460
00714196312662	00312E
00714196312402	31240
00714196311108	31110
00714196219442	00219E
00714196391704	31110
00714196391681	31460
00714196391605	00312E
00714196391582	00219E
00714196391568	31240