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RZ Medizintechnik GmbH

FDA UDI

Class II (US FDA UDI)

by RZ-Medizintechnik GmbH

Identity

Trade Name
RZ Medizintechnik GmbH FDA UDI
Generic Name
Endoscopic electrosurgical handpiece/electrode, monopolar, reusable FDA UDI
Device Name
Outer Shaft Ø5mm, insulated, WL 330mm adaptable to all Handles FDA UDI
Model / Reference
300-660-005 FDA UDI
Description
Outer Shaft Ø5mm, insulated, WL 330mm adaptable to all Handles FDA UDI

Identifiers

Catalog Number
300-660-005 FDA UDI
Primary DI / UDI-DI
04049197406987 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Endoscopic electrosurgical handpiece/electrode, monopolar, reusable 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Endoscopic electrosurgical handpiece/electrode, monopolar, reusable

RZ Medizintechnik GmbH by RZ-Medizintechnik GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic electrosurgical handpiece/electrode, monopolar, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
RZ-Medizintechnik GmbH

Sources (1)

  • FDA UDI a3955e84-3970-4326-90b1-9590b62f133d 35 fields · synced May 30, 2026