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Multi-RF Therapy Cable

FDA UDI

Class II (US FDA UDI)

by Avanos Medical, Inc.

Identity

Trade Name
Multi-RF Therapy Cable FDA UDI
Generic Name
Electrosurgical cable adaptor FDA UDI
Device Name
Multi-RF Therapy Cable FDA UDI
Model / Reference
SRX-CRG-MRF FDA UDI
Description
Multi-RF Therapy Cable FDA UDI

Identifiers

Catalog Number
SRX-CRG-MRF FDA UDI
Primary DI / UDI-DI
00193493473069 FDA UDI
510(k) Number
K192491 FDA UDI
FDA Product Code
GXD FDA UDI
GMDN Term
Electrosurgical cable adaptor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4400 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrosurgical cable adaptor

Multi-RF Therapy Cable by Avanos Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrosurgical cable adaptor.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4705c635-ad9b-4570-9084-957819117965 36 fields · synced Jun 9, 2026