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Dyonics 25

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
DYONICS 25 FDA UDI
Generic Name
Endoscopic device remote control FDA UDI
Device Name
SVCE REPL DYONICS 25 WIRELESS REMOTE FDA UDI
Model / Reference
72200891SR FDA UDI
Description
SVCE REPL DYONICS 25 WIRELESS REMOTE FDA UDI

Identifiers

Catalog Number
72200891SR FDA UDI
Primary DI / UDI-DI
00885556632611 FDA UDI
FDA Product Code
HRX FDA UDI
GMDN Term
Endoscopic device remote control 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

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: Endoscopic device remote control

Dyonics 25 by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic device remote control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d0953a94-c834-4519-b62e-70198c6bf398 35 fields · synced Jun 8, 2026