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Dyonics

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
DYONICS FDA UDI
Generic Name
Arthroscopic shaver system, electrically-powered FDA UDI
Device Name
RFB 3RD EDITION C/U DYONICS PWR II FDA UDI
Model / Reference
72200873F3E FDA UDI
Description
RFB 3RD EDITION C/U DYONICS PWR II FDA UDI

Identifiers

Catalog Number
72200873F3E FDA UDI
Primary DI / UDI-DI
00885554030808 FDA UDI
FDA Product Code
HRX FDA UDI
GMDN Term
Arthroscopic shaver system, electrically-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.1100 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Arthroscopic shaver system, electrically-powered

Dyonics by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arthroscopic shaver system, electrically-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Smith & Nephew, Inc.

Sources (1)

  • FDA UDI 8faa1eac-f64c-482b-bbf0-e1a448f65d1c 35 fields · synced Jun 8, 2026