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Sontek Medical A1003 Case

by Nextphase Medical Devices LLC

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00859758005047 UDI-DI Date20 Feb 2025ListedStatusListed 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  • Withdrawn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
Sontek Medical
Generic Name
Anaesthesia breathing circuit, single-use
Model / Reference
A1003 Case
Primary DI / UDI-DI
00859758005047
FDA Product Code
BZA
GMDN Term
Anaesthesia breathing circuit, single-use
Device Class
Class I
Regulation Number
868.5810
GUDID distribution status
In Commercial Distribution

Related devices

Category: Anaesthesia breathing circuit, single-use

Other devices from Nextphase Medical Devices LLC

See all devices from Nextphase Medical Devices LLC →

Properties

  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No