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11540AA

by Karl Storz SE & CO. KG

11540AA is a device classified as Unclassified made by Karl Storz SE & CO. KG, listed in FDA GUDID since 24 Sep 2014 (UDI-DI 04048551227046), 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 Number04048551227046 UDI-DI Date24 Sep 2014ListedStatusListed 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  • Withdrawn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 fibreoptic hysteroscope
Model / reference
11540AA
Primary DI / UDI-DI
04048551227046
FDA product code
HFA
GMDN term
Flexible fibreoptic hysteroscope
Device class
Unclassified
Regulation number
884.1600
GUDID distribution status
In Commercial Distribution

Related devices

Category: Flexible fibreoptic hysteroscope

Other devices from Karl Storz SE & CO. KG

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Properties

  • Sterilise before use
  • Prescription use
  • Serial number
Other properties (12, all answered No)