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Dukal 5530

by Dukal LLC

Dukal 5530 is a Class I device made by Dukal LLC, listed in FDA GUDID since 26 Feb 2026 (UDI-DI 10665973033027), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10665973033027 UDI-DI Date26 Feb 2026ListedStatusListed 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  • Withdrawn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
Non-woven gauze pad
Model / Ref / Catalog
5530
Primary DI / UDI-DI
10665973033027
FDA product code
NAC
GMDN term
Non-woven gauze pad
Device class
Class I
Regulation number
878.4018
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code NAC (Dressing, wound, hydrophilic).

Other devices from Dukal LLC

See all devices from Dukal LLC →

Properties

  • Supplied sterile
  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (10, all answered No)