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Vertebris

FDA UDI

Class I (US FDA UDI)

by Richard Wolf GmbH

Identity

Trade Name
VERTEBRIS FDA UDI
Generic Name
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI
Device Name
NUCLEUS GRASP. FORCEPS Ø 4MM WL 360MM color code yellow, TL 470 mm, with irrigation connection, reusable FDA UDI
Model / Reference
892301004 FDA UDI
Description
NUCLEUS GRASP. FORCEPS Ø 4MM WL 360MM color code yellow, TL 470 mm, with irrigation connection, reusable FDA UDI

Identifiers

Catalog Number
89230.1004 FDA UDI
Primary DI / UDI-DI
04055207035375 FDA UDI
FDA Product Code
NBH FDA UDI
GMDN Term
Rigid endoscopic tissue manipulation forceps, reusable 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
Outer Diameter — 4 Millimeter FDA UDI
Length — 360 Millimeter FDA UDI

Category: Rigid endoscopic tissue manipulation forceps, reusable

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

Similar devices

Also classified as Rigid endoscopic tissue manipulation forceps, reusable.

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 345f0669-e955-4d4a-b4a8-640381062cb6 37 fields · synced May 30, 2026