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Resonance RE-VO2

by M.R.S. SRL

Resonance RE-VO2 (4300103520) is a Class I device made by M.R.S. SRL, listed in FDA GUDID since 3 Sep 2025 (UDI-DI 08051597160501), 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 Number08051597160501 UDI-DI Date3 Sep 2025ListedStatusListed 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  • Withdrawn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
Resonance
Generic name
Video otoscope/audiometer
Model / Ref / Catalog
RE-VO2, 4300103520
Primary DI / UDI-DI
08051597160501
FDA product code
ERA
GMDN term
Video otoscope/audiometer
Device class
Class I
Regulation number
874.4770
GUDID distribution status
In Commercial Distribution

Related devices

Category: Video otoscope/audiometer

Similar devices

Also classified as Video otoscope/audiometer.

Similar devices

Other devices filed under FDA product code ERA (Otoscope).

Other devices from M.R.S. SRL

Properties

  • Single use
  • Premarket exempt
  • Serial number
Other properties (12, all answered No)