RZ Medizintechnik GmbH

FDA UDI

Class I (US FDA UDI)

by RZ-Medizintechnik GmbH

Identity

Trade Name: RZ Medizintechnik GmbH FDA UDI
Generic Name: Bone lever/elevator, reusable FDA UDI
Device Name: Jaboma Cleft Palate Periosteal Elevator curved, 170mm, 6 3/4'' FDA UDI
Model / Reference: 431-200-100 FDA UDI
Description: Jaboma Cleft Palate Periosteal Elevator curved, 170mm, 6 3/4'' FDA UDI

Identifiers

Catalog Number: 431-200-100 FDA UDI
Primary DI / UDI-DI: 04049197322928 FDA UDI
FDA Product Code: LRC FDA UDI
GMDN Term: Bone lever/elevator, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 874.4420 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Bone lever/elevator, reusable

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

Similar devices

Also classified as Bone lever/elevator, reusable.

Arthrex® — Arthrex, Inc. · Class I
General Instruments — ALPHATEC SPINE, INC. · Class I
IdentiTi — ALPHATEC SPINE, INC. · Class I
Intervertebral Disc Preparation Instruments — ALPHATEC SPINE, INC. · Class I
HAT-TRICK — Smith & Nephew, Inc. · Class I
ORTHOMED — ORTHO-MED, INC. · Class I
Symmetry Allerdyce — SYMMETRY SURGICAL INC. · Class I
Life Instruments — Life Instrument Corporation · Class I

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 I	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: RZ-Medizintechnik GmbH

Sources (1)

FDA UDI 9bdbae93-ea60-4bd3-a0d4-071483a20407 35 fields · synced May 30, 2026