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b.pure 64430233EB

by Fourstar Group Inc.

b.pure 64430233EB is a Class I device made by Fourstar Group Inc., listed in FDA GUDID since 5 Feb 2023 (UDI-DI 00049696889520), 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 Number00049696889520 UDI-DI Date5 Feb 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  • Withdrawn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
b.pure
Generic name
Skin surface device adhesive
Model / reference
64430233EB
Primary DI / UDI-DI
00049696889520
FDA product code
NAC
GMDN term
Skin surface device adhesive
Device class
Class I
Regulation number
878.4018
GUDID distribution status
In Commercial Distribution

Related devices

Category: Skin surface device adhesive

Similar devices

Other devices filed under FDA product code NAC (Dressing, Wound, Hydrophilic).

Other devices from Fourstar Group Inc.

See all devices from Fourstar Group Inc. →

Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)