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Acteon Tip RHS3L M+ Sterile

by Satelec

Acteon Tip RHS3L M+ Sterile (F87991) is a Class II device made by Satelec, listed in FDA GUDID since 23 Dec 2019 (UDI-DI 03609820879918), 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 Number03609820879918 UDI-DI Date23 Dec 2019ListedStatusListed 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  • Withdrawn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
Acteon
Generic name
Hard/soft-tissue ultrasonic surgical system
Model / Ref / Catalog
TIP RHS3L M+ STERILE, F87991
Primary DI / UDI-DI
03609820879918
FDA product code
JDX
GMDN term
Hard/soft-tissue ultrasonic surgical system
Device class
Class II
Regulation number
888.4580
GUDID distribution status
In Commercial Distribution

Related devices

Category: Hard/soft-tissue ultrasonic surgical system

Similar devices in this category

Other devices filed under Hard/soft-tissue ultrasonic surgical system.

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)