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Dukal 27612

by Dukal LLC

Dukal 27612 is a Class I device made by Dukal LLC, listed in FDA GUDID since 6 Dec 2022 (UDI-DI 10665973027293), not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 Number10665973027293 UDI-DI Date6 Dec 2022ListedStatusListed GUDID: not 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  • Withdrawn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
Medical equipment/instrument drape, single-use
Model / Ref / Catalog
27612
Primary DI / UDI-DI
10665973027293
FDA product code
NRD
GMDN term
Medical equipment/instrument drape, single-use
Device class
Class I
Regulation number
872.6640
GUDID distribution status
Not in Commercial Distribution

Other devices from Dukal LLC

See all devices from Dukal LLC →

Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)