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Flex-X 11278AC2

by Karl Storz SE & CO. KG United States GUDID

Product code FGB

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04048551402504 UDI-DIDate23 Sep 2016ListedStatusIn distribution

Coverage

1 jurisdiction

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  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls: none on record (FDA, checked 22 Oct 2026)

Specification

GUDID · synced 22 Oct 2026

Trade Name
Flex-X
Generic Name
Flexible fibreoptic cystourethroscope
Model / Reference
11278AC2
Primary DI / UDI-DI
04048551402504
FDA Product Code
FGB
GMDN Term
Flexible fibreoptic cystourethroscope
Device Class
Class II
Regulation Number
876.1500
Commercial Distribution
In Commercial Distribution
Sterilization Method
Ethylene Oxide

Other devices from Karl Storz SE & CO. KG

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Properties & raw data

Show properties, registry sources and raw records
  • Prescription Use
  • Serial Number
Other properties (12)
  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No

Sources (1)

  • FDA UDI a0a41a7d-175a-482a-a4a1-60db129a9848 33 fields · synced 22 Oct 2026