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TORS Series 1

by Radley Scientific Limited 67 variants

TORS Series 1 (P6N2) is a Class II device made by Radley Scientific Limited, listed in FDA GUDID since 19 Nov 2025 (UDI-DI 05060634771788), 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 Number05060634771788 UDI-DI Date19 Nov 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  • Withdrawn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
Tors
Generic name
Hard/soft-tissue ultrasonic surgical system
Model / Ref / Catalog
Series 1, P6N2
Primary DI / UDI-DI
05060634771788
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
Sterilisation method
Moist Heat or Steam Sterilization
Size
Length — 200 Millimeter
Outer Diameter — 6 Millimeter

Other devices from Radley Scientific Limited

See all devices from Radley Scientific Limited →

Properties

  • Sterilise before use
  • Single use
  • Prescription use
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (9, all answered No)