Dukal 16700

Dukal 16700 is a Class I device made by Dukal LLC, listed in FDA GUDID since 6 Dec 2022 (UDI-DI 10665973019908), 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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number10665973019908 UDI-DI	Date6 Dec 2022Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 10665973019908

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Dukal
Generic name: Skin-cover adhesive strip, non-antimicrobial
Model / Ref / Catalog: 16700

Primary DI / UDI-DI: 10665973019908
FDA product code: KGX
GMDN term: Skin-cover adhesive strip, non-antimicrobial

Device class: Class I
Regulation number: 880.5240
GUDID distribution status: In Commercial Distribution

Similar devices in this category

Other devices filed under Skin-cover adhesive strip, non-antimicrobial.

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Properties

Supplied sterile
Single use
Over-the-counter
Premarket exempt
Lot / batch number

Other properties (10, all answered No)