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RZ Medizintechnik GmbH

FDA UDI

Class I (US FDA UDI)

by RZ-Medizintechnik GmbH

Identity

Trade Name
RZ Medizintechnik GmbH FDA UDI
Generic Name
Magnetic surgical manipulation system instrument, external, permanent magnet FDA UDI
Device Name
MICS Magnetic Retriever 370mm, 14 1/2" FDA UDI
Model / Reference
295-300-000 FDA UDI
Description
MICS Magnetic Retriever 370mm, 14 1/2" FDA UDI

Identifiers

Catalog Number
295-300-000 FDA UDI
Primary DI / UDI-DI
04049197508285 FDA UDI
FDA Product Code
DWS FDA UDI
GMDN Term
Magnetic surgical manipulation system instrument, external, permanent magnet FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.4500 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Magnetic surgical manipulation system instrument, external, permanent magnet

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

Similar devices

Also classified as Magnetic surgical manipulation system instrument, external, permanent magnet.

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 c31e6441-132d-4ffa-aca9-a2f358f09108 35 fields · synced May 31, 2026