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Megadyne

FDA UDI

Class II (US FDA UDI)

by Megadyne Medical Products, Inc.

Identity

Trade Name
Megadyne FDA UDI
Generic Name
Electrosurgical return electrode, single-use FDA UDI
Device Name
Patient Return Electrode, Single Use, Contact Quality Monitoring, Adult With 9 ft (2.7 m) Cord. For Patients Weighing Over 33lbs. (15kg) FDA UDI
Model / Reference
0855CN FDA UDI
Description
Patient Return Electrode, Single Use, Contact Quality Monitoring, Adult With 9 ft (2.7 m) Cord. For Patients Weighing Over 33lbs. (15kg) FDA UDI

Identifiers

Catalog Number
0855CN FDA UDI
Primary DI / UDI-DI
10614559104613 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrosurgical return electrode, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrosurgical return electrode, single-use

Megadyne by Megadyne Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrosurgical return electrode, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 22df1e35-201c-4b4f-ac99-e4322730ba1d 36 fields · synced Jun 9, 2026