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VBR™ vertebral body replacement

FDA UDI

Class II (US FDA UDI)

by Ulrich GmbH & Co. KG

Identity

Trade Name
VBR™ vertebral body replacement FDA UDI
Generic Name
Vertebral body prosthesis FDA UDI
Device Name
VBR end piece, size S, left, 8° FDA UDI
Model / Reference
CS 2228-821306 FDA UDI
Description
VBR end piece, size S, left, 8° FDA UDI

Identifiers

Catalog Number
CS 2228-821306 FDA UDI
Primary DI / UDI-DI
04052536076161 FDA UDI
FDA Product Code
MQP FDA UDI
GMDN Term
Vertebral body prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Conditional FDA UDI

VBR™ vertebral body replacement by Ulrich GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ulrich GmbH & Co. KG

Sources (1)

  • FDA UDI b6e27cdd-b1b5-43a4-8eac-709f9173ec23 36 fields · synced Jun 7, 2026