Rongeur, Conchotome, for decalcification 30cm 3mm 30° upwards

FDA UDI

Class I (US FDA UDI)

by Geister Medizin Technik GmbH

Identity

Trade Name: Rongeur, Conchotome, for decalcification 30cm 3mm 30° upwards FDA UDI
Generic Name: Spinal rongeur FDA UDI
Device Name: Rongeur, Conchotome, for decalcification 30cm 3mm 30° upwards ValveGate™ FDA UDI
Model / Reference: 34-7451 FDA UDI
Description: Rongeur, Conchotome, for decalcification 30cm 3mm 30° upwards ValveGate™ FDA UDI

Identifiers

Catalog Number: 34-7451 FDA UDI
Primary DI / UDI-DI: 04057034120255 FDA UDI
FDA Product Code: HTX FDA UDI
GMDN Term: Spinal rongeur FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.4540 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

Category: Spinal rongeur

Rongeur, Conchotome, for decalcification 30cm 3mm 30° upwards by Geister Medizin Technik GmbH — Class I — FDA UDI — listed in FDA GUDID

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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

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Manufacturer

Manufacturer: Geister Medizin Technik GmbH

Sources (1)

FDA UDI 2c0f82c1-ee0a-4922-843b-9085a227e603 35 fields · synced May 31, 2026