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Dyonics / Hermes

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
DYONICS / HERMES FDA UDI
Generic Name
Arthroscopic shaver system, electrically-powered FDA UDI
Device Name
DYONICS POWER HERMES U.K. KIT FDA UDI
Model / Reference
7210194 FDA UDI
Description
DYONICS POWER HERMES U.K. KIT FDA UDI

Identifiers

Catalog Number
7210194 FDA UDI
Primary DI / UDI-DI
00885554011449 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Arthroscopic shaver system, electrically-powered

Dyonics / Hermes 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 55174554-f117-4dd3-92b1-52f93a14ffd4 35 fields · synced Jun 8, 2026