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Tors

FDA UDI

Class II (US FDA UDI)

by Radley Scientific Limited

Identity

Trade Name
TORS FDA UDI
Generic Name
Hard/soft-tissue ultrasonic surgical system FDA UDI
Device Name
S8S2 - Cement 200 DIA 8 Scraper Probe (Single Use - Sterile) FDA UDI
Model / Reference
Series 1 FDA UDI
Description
S8S2 - Cement 200 DIA 8 Scraper Probe (Single Use - Sterile) FDA UDI

Identifiers

Catalog Number
S8S2 FDA UDI
Primary DI / UDI-DI
05060634770552 FDA UDI
FDA Product Code
JDX FDA UDI
GMDN Term
Hard/soft-tissue ultrasonic surgical system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.4580 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 200 Millimeter FDA UDI
Outer Diameter — 8 Millimeter FDA UDI

Category: Hard/soft-tissue ultrasonic surgical system

Tors by Radley Scientific Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hard/soft-tissue ultrasonic surgical system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cce969c2-a7c1-4a9a-a505-50aa9ea3065b 36 fields · synced May 30, 2026