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Highflow 2235611

by Richard Wolf GmbH

Highflow 2235611 is a Class II device made by Richard Wolf GmbH, listed in FDA GUDID since 21 Jul 2017 (UDI-DI 04055207056592), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04055207056592 UDI-DI Date21 Jul 2017ListedStatusListed 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  • Withdrawn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
Highflow
Generic name
Laparoscopic insufflator
Model / Ref / Catalog
2235611
Primary DI / UDI-DI
04055207056592
FDA product code
HIF
GMDN term
Laparoscopic insufflator
Device class
Class II
Regulation number
884.1730
GUDID distribution status
In Commercial Distribution

Related devices

Category: Laparoscopic insufflator

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Other devices filed under Laparoscopic insufflator.

Other devices from Richard Wolf GmbH

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Properties

  • Serial number
  • Manufacturing date
Other properties (13, all answered No)