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Olympus

FDA UDI

Class II (US FDA UDI)

by Modern Medical Equipment MFG. Ltd.

Identity

Trade Name
Olympus FDA UDI
Generic Name
Endoscopic electrosurgical electrode, monopolar, single-use FDA UDI
Device Name
Disposable Lap. Electrodes, J Hook, Wire, 33cm,2.36mm Shaft,Teflon Coated FDA UDI
Model / Reference
WA98910E FDA UDI
Description
Disposable Lap. Electrodes, J Hook, Wire, 33cm,2.36mm Shaft,Teflon Coated FDA UDI

Identifiers

Primary DI / UDI-DI
06939029817020 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Endoscopic electrosurgical electrode, monopolar, 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

Yes

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: Endoscopic electrosurgical electrode, monopolar, single-use

Olympus by Modern Medical Equipment MFG. Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic electrosurgical electrode, monopolar, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b010652e-e023-408a-aa27-460048aa1a3b 33 fields · synced May 30, 2026