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Flowmeter Manifold IV Pole

by Maxtec, Inc. 2 variants

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 Number00817770025757 UDI-DI Date8 Jun 2023ListedStatusListed 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  • Withdrawn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
Flowmeter Manifold
Generic name
Medical gas flowmeter, Thorpe tube
Model / Ref / Catalog
IV Pole, R220P10-009
Primary DI / UDI-DI
00817770025757
FDA product code
CAX
GMDN term
Medical gas flowmeter, Thorpe tube
Device class
Class I
Regulation number
868.2340
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Related devices

Category: Medical gas flowmeter, Thorpe tube

Other devices from Maxtec, Inc.

See all devices from Maxtec, Inc. →

Properties

  • Premarket exempt
  • Lot / batch number
  • Manufacturing date

Other properties (12)

  • Supplied sterile: No
  • Sterilise before use: 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
  • Serial number: No
  • Expiration date: No