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Pediatric Ultra Flex® J21814-13621

by King Systems Corporation.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00612649217680 UDI-DI Date21 Aug 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Pediatric Ultra Flex®
Generic Name
Anaesthesia breathing circuit, single-use
Model / Ref / Catalog
J21814-13621
Primary DI / UDI-DI
00612649217680
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

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 (7)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No