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Carrera Loop Electrode

FDA UDI

Class II (US FDA UDI)

by Gynex Corporation

Identity

Trade Name
Carrera Loop Electrode FDA UDI
Generic Name
Electrocautery system electrode FDA UDI
Model / Reference
CMB-2-3-2 FDA UDI

Identifiers

Primary DI / UDI-DI
GYNXCMB2321 FDA UDI
510(k) Number
K982739 FDA UDI
FDA Product Code
HGI FDA UDI
GMDN Term
Electrocautery system electrode FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.4120 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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: Electrocautery system electrode

Carrera Loop Electrode by Gynex Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocautery system electrode.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gynex Corporation

Sources (1)

  • FDA UDI 3060867b-a1cd-47f6-a9e6-8cd15b14f48a 33 fields · synced May 30, 2026