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11540KD

by Karl Storz SE & CO. KG

11540KD is a Class II device made by Karl Storz SE & CO. KG, listed in FDA GUDID since 21 Aug 2018 (UDI-DI 04048551051429), 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 Number04048551051429 UDI-DI Date21 Aug 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  • Withdrawn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

Generic name
Flexible endoscopic biopsy handpiece/needle
Model / Ref / Catalog
11540KD
Primary DI / UDI-DI
04048551051429
FDA product code
HET
GMDN term
Flexible endoscopic biopsy handpiece/needle
Device class
Class II
Regulation number
884.1720
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Flexible endoscopic biopsy handpiece/needle

Similar devices

Other devices filed under FDA product code HET (LAPAROSCOPE, GYNECOLOGIC (AND ACCESSORIES)).

Other devices from Karl Storz SE & CO. KG

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Properties

  • Sterilise before use
  • Single use
  • Prescription use
  • Lot / batch number
Other properties (11, all answered No)