Vertebris

FDA UDI

Class I (US FDA UDI)

by Richard Wolf GmbH

Identity

Trade Name: VERTEBRIS FDA UDI
Generic Name: Spinal rongeur FDA UDI
Device Name: INTRADISC FORCEPS Ø 5.2MM WL 240MM color code white, articulating, TL 389mm, with irrigation connection, reusable FDA UDI
Model / Reference: 892401052 FDA UDI
Description: INTRADISC FORCEPS Ø 5.2MM WL 240MM color code white, articulating, TL 389mm, with irrigation connection, reusable FDA UDI

Identifiers

Catalog Number: 89240.1052 FDA UDI
Primary DI / UDI-DI: 04055207046906 FDA UDI
FDA Product Code: NBH FDA UDI
GMDN Term: Spinal rongeur FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.1100 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

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

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Length — 240 Millimeter FDA UDI
Outer Diameter — 5.2 Millimeter FDA UDI

Category: Spinal rongeur

Vertebris by Richard Wolf GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal rongeur.

Avalign — AVALIGN TECHNOLOGIES, Inc. · Class II
Sklar — Sklar Corporation · Class I
Avalign — AVALIGN TECHNOLOGIES, Inc. · Class II
Millennium — AVALIGN TECHNOLOGIES, Inc. · Class II
Millennium — AVALIGN TECHNOLOGIES, Inc. · Class II
Medicon — Medicon eG. Chirurgiemechaniker-Genossenschaft · Class I
V. Mueller — STERIS CORPORATION · Class II
Boss Instruments — Boss Instruments, Ltd. · Class II

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: Richard Wolf GmbH

Sources (1)

FDA UDI 2ad16aa5-6138-4f17-b44e-2bf46e868094 36 fields · synced May 31, 2026