← Back to catalogue

Adapter, Wolf/Dyonics

FDA UDI

Class I (US FDA UDI)

by Clarus Medical, Llc

Identity

Trade Name
Adapter, Wolf/Dyonics FDA UDI
Generic Name
Fibreoptic light cable FDA UDI
Device Name
Adapter, Wolf/Dyonics FDA UDI
Model / Reference
5196-904 FDA UDI
Description
Adapter, Wolf/Dyonics FDA UDI

Identifiers

Catalog Number
5196-904 FDA UDI
Primary DI / UDI-DI
10810004820736 FDA UDI
FDA Product Code
FEM FDA UDI
GMDN Term
Fibreoptic light cable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.1500 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Fibreoptic light cable

Adapter, Wolf/Dyonics by Clarus Medical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fibreoptic light cable.

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
Clarus Medical, Llc

Sources (1)

  • FDA UDI dcc3c900-342d-4b0d-8f82-001240b3bb10 35 fields · synced May 30, 2026