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Dukal 7007101

by Dukal LLC

Dukal 7007101 is a Class I device made by Dukal LLC, listed in FDA GUDID since 29 Aug 2023 (UDI-DI 00665973031675), 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 Number00665973031675 UDI-DI Date29 Aug 2023ListedStatusListed 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  • Withdrawn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
Dukal
Generic name
Synthetic polymer burn dressing, gel-coated
Model / Ref / Catalog
7007101
Primary DI / UDI-DI
00665973031675
FDA product code
NAE
GMDN term
Synthetic polymer burn dressing, gel-coated
Device class
Class I
Regulation number
878.4022
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code NAE (Dressing, wound, hydrogel without drug and/or biologic).

Other devices from Dukal LLC

See all devices from Dukal LLC →

Properties

  • Supplied sterile
  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)