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Biopsy Kit for 10G Vertebroplasty Needle Kit

FDA UDI

Class I (US FDA UDI)

by Möller Medical GmbH

Identity

Trade Name
Biopsy Kit for 10G Vertebroplasty Needle Kit FDA UDI
Generic Name
Vertebral bone biopsy needle FDA UDI
Device Name
The biopsy kit for the Synthes Vertecem / Vertecem V + system is a sterile packed kit for taking bone biopsies from the vertebral body. FDA UDI
Model / Reference
10001573US FDA UDI
Description
The biopsy kit for the Synthes Vertecem / Vertecem V + system is a sterile packed kit for taking bone biopsies from the vertebral body. FDA UDI

Identifiers

Catalog Number
03.702.223S FDA UDI
Primary DI / UDI-DI
04260277175627 FDA UDI
FDA Product Code
MJG FDA UDI
GMDN Term
Vertebral bone biopsy needle FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vertebral bone biopsy needle

Biopsy Kit for 10G Vertebroplasty Needle Kit by Möller Medical GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vertebral bone biopsy needle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Möller Medical GmbH

Sources (1)

  • FDA UDI c30787a1-161e-48fa-8962-c08a5e7c8132 34 fields · synced Jun 9, 2026