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Boa 7355071US

by Richard Wolf GmbH

Boa 7355071US is a flexible video ureterorenoscope (FDA Class II) made by Richard Wolf GmbH, listed in FDA GUDID since 15 Jul 2021 (UDI-DI 00814334022825), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00814334022825 UDI-DI Date15 Jul 2021ListedStatusListed 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  • Withdrawn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
Boa
Generic name
Flexible video ureterorenoscope, reusable
Model / Ref / Catalog
7355071US
Primary DI / UDI-DI
00814334022825
FDA product code
FGA, FGB
GMDN term
Flexible video ureterorenoscope, reusable
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution
Sterilisation method
Hydrogen Peroxide
Size
Outer Diameter — 2.9 Millimeter
Length — 680 Millimeter

Related devices

Category: Flexible video ureterorenoscope, reusable

Other devices from Richard Wolf GmbH

See all devices from Richard Wolf GmbH →

Properties

  • Sterilise before use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)