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DermaGinate/Ag 00520E

by Sion Brands LLC 2 variants

DermaGinate/Ag 00520E is a device classified as Unclassified made by Sion Brands LLC, listed in FDA GUDID since 1 Sep 2020 (UDI-DI 00714196520227), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00714196520227 UDI-DI Date1 Sep 2020ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
DermaGinate/Ag
Generic name
Exudate-absorbent dressing, hydrophilic-gel, antimicrobial
Model / reference
00520E
Primary DI / UDI-DI
00714196520227
FDA product code
FRO
GMDN term
Exudate-absorbent dressing, hydrophilic-gel, antimicrobial
Device class
U
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code FRO (Dressing, Wound, Drug).

Other devices from Sion Brands LLC

See all devices from Sion Brands LLC →

Properties

  • Supplied sterile
  • Single use
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)