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Universal FLEX2® F99008

by King Systems Corporation

Universal FLEX2® F99008 is a Class I device made by King Systems Corporation, listed in FDA GUDID since 13 Dec 2022 (UDI-DI 00612649215013), registry data as of 8 Nov 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00612649215013 UDI-DI Date13 Dec 2022ListedStatusListed 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  • Withdrawn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
Universal FLEX2®
Generic name
Anaesthesia breathing circuit, single-use
Model / Ref / Catalog
F99008
Primary DI / UDI-DI
00612649215013
FDA product code
CAI
GMDN term
Anaesthesia breathing circuit, single-use
Device class
Class I
Regulation number
868.5240
GUDID distribution status
In Commercial Distribution

Related devices

Category: Anaesthesia breathing circuit, single-use

Other devices from King Systems Corporation

See all devices from King Systems Corporation →

Properties

  • Single use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)