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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
RONGEUR 4.3X5MM WL 247MM jaw section 6mm long, TL 320mm, reusable FDA UDI
Model / Reference
8791691 FDA UDI
Description
RONGEUR 4.3X5MM WL 247MM jaw section 6mm long, TL 320mm, reusable FDA UDI

Identifiers

Catalog Number
8791.691 FDA UDI
Primary DI / UDI-DI
04055207043134 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 247 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.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Richard Wolf GmbH

Sources (1)

  • FDA UDI be2f4080-5016-4e82-b94c-36179fbe847b 36 fields · synced Jun 1, 2026