← Back to catalogue

Dyonics Power Ii

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
DYONICS POWER II FDA UDI
Generic Name
Insufflation gas conditioning system control unit FDA UDI
Device Name
DII CONTROLLER FDA UDI
Model / Reference
72200873 FDA UDI
Description
DII CONTROLLER FDA UDI

Identifiers

Catalog Number
72200873 FDA UDI
Primary DI / UDI-DI
03596010607409 FDA UDI
FDA Product Code
HRX FDA UDI
GMDN Term
Insufflation gas conditioning system control unit 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: Insufflation gas conditioning system control unit

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

Similar devices

Also classified as Insufflation gas conditioning system control unit.

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 b5504dbf-ef34-4c70-873a-711453fb9116 35 fields · synced Jun 8, 2026