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B.I.O.H. 26252BO

by Karl Storz SE & CO. KG

B.I.O.H. 26252BO is a Class II device made by Karl Storz SE & CO. KG, listed in FDA GUDID since 21 Jul 2018 (UDI-DI 04048551257388), 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 Number04048551257388 UDI-DI Date21 Jul 2018ListedStatusListed 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  • Withdrawn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.I.O.H.
Generic name
Endoscope sheath, reusable
Model / reference
26252BO
Primary DI / UDI-DI
04048551257388
FDA product code
HIH
GMDN term
Endoscope sheath, reusable
Device class
Class II
Regulation number
884.1690
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Endoscope sheath, reusable

Other devices from Karl Storz SE & CO. KG

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Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)