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BContak B1693

by Bridon, Corp. 2 variants

BContak B1693 (B1754) is a Class III device made by Bridon, Corp., listed in FDA GUDID since 8 Apr 2024 (UDI-DI 00850023087973), 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 Number00850023087973 UDI-DI Date8 Apr 2024ListedStatusListed 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  • Withdrawn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
BContak
Generic name
Skin-closure adhesive strip
Model / Ref / Catalog
B1693, B1754
Primary DI / UDI-DI
00850023087973
FDA product code
KGM
GMDN term
Skin-closure adhesive strip
Device class
Class III
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide

Related devices

Category: Skin-closure adhesive strip

Other devices from Bridon, Corp.

Properties

  • Supplied sterile
  • Sterilise before use
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)