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Analgesia Gas Mixer, Digital Mdm Delivery System 40151601 Kor

by Parker Hannifin Corp.

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

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 Number00816711020097 UDI-DI Date24 Sep 2025ListedStatusListed GUDID: not in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Analgesia Gas Mixer, Digital Mdm Delivery System
Generic Name
Oxygen/air/nitrous oxide breathing gas mixer
Model / Reference
40151601 KOR
Primary DI / UDI-DI
00816711020097
510(k) Number
FDA Product Code
BSZ
GMDN Term
Oxygen/air/nitrous oxide breathing gas mixer
Device Class
Class II
Regulation Number
868.5160
GUDID distribution status
Not in Commercial Distribution

Related devices

Cleared under the same submission (K884879)

Show all (12)

Other devices from Parker Hannifin Corp.

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Properties

  • Serial Number

Other properties (13)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: 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