Stryker

FDA UDI

Class II (US FDA UDI)

by Nissha Medical Technologies Sas

Identity

Trade Name: Stryker FDA UDI
Generic Name: Electrosurgical return electrode, single-use FDA UDI
Device Name: Neutral Electrodes intended to be used in combination with the device “Stryker MultiGen 2 RF Generator” FDA UDI
Model / Reference: 0406-650-205 FDA UDI
Description: Neutral Electrodes intended to be used in combination with the device “Stryker MultiGen 2 RF Generator” FDA UDI

Identifiers

Catalog Number: 700000856 FDA UDI
Primary DI / UDI-DI: 15060842920029 FDA UDI
510(k) Number: K203494 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Electrosurgical return electrode, single-use

Stryker by Nissha Medical Technologies Sas — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Nissha Medical Technologies Sas

Sources (1)

FDA UDI 3922d9b4-db1b-482f-b43d-5f54892a956d 36 fields · synced May 31, 2026