← Back to catalogue

Dyonics Power

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
DYONICS POWER FDA UDI
Generic Name
Multi-purpose surgical power tool system, line-powered FDA UDI
Device Name
DYONICS POWER DRILL FDA UDI
Model / Reference
7205785 FDA UDI
Description
DYONICS POWER DRILL FDA UDI

Identifiers

Catalog Number
7205785 FDA UDI
Primary DI / UDI-DI
03596010410702 FDA UDI
FDA Product Code
HAB FDA UDI
GMDN Term
Multi-purpose surgical power tool system, line-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Multi-purpose surgical power tool system, line-powered

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

Similar devices

Also classified as Multi-purpose surgical power tool system, line-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Smith & Nephew, Inc.

Sources (1)

  • FDA UDI 4cd0f671-75df-4bce-a5f1-c85a91eda82e 35 fields · synced Jun 8, 2026