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Fisher & Paykel Healthcare 9420012402691

by Fisher & Paykel Healthcare, Inc.

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 Number09420012402691 UDI-DI Date26 Mar 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  • Withdrawn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
Fisher & Paykel Healthcare
Generic Name
Inspiratory/expiratory limb respiratory tubing, reusable
Model / Ref / Catalog
9420012402691
Primary DI / UDI-DI
09420012402691
FDA Product Code
BZO
GMDN Term
Inspiratory/expiratory limb respiratory tubing, reusable
Device Class
Class I
Regulation Number
868.5975
GUDID distribution status
In Commercial Distribution

Other devices from Fisher & Paykel Healthcare, Inc.

See all devices from Fisher & Paykel Healthcare, Inc. →

Properties

  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

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