BiopsyPointer 190

FDA UDI

Class II (US FDA UDI)

by Fiagon GmbH

Identity

Trade Name: BiopsyPointer 190 FDA UDI
Generic Name: Multi-purpose stereotactic surgery system FDA UDI
Device Name: The products BiopsyPointer 190 referred to as BiopsyPointer is a product variant for the navigation of neurosurgical brain biopsy cannulas. The instruments are accessories to the Fiagon Navigation system. The instruments in connection with the Navigation system are indicated for any medical condition in which the use of stereotactic surgery may be appropriate, and where reference to a rigid anatomical structure in the field of cranial surgery can be identified relative to a CT or MR based model of the anatomy. FDA UDI
Model / Reference: 1 FDA UDI
Description: The products BiopsyPointer 190 referred to as BiopsyPointer is a product variant for the navigation of neurosurgical brain biopsy cannulas. The instruments are accessories to the Fiagon Navigation system. The instruments in connection with the Navigation system are indicated for any medical condition in which the use of stereotactic surgery may be appropriate, and where reference to a rigid anatomical structure in the field of cranial surgery can be identified relative to a CT or MR based model of the anatomy. FDA UDI

Identifiers

Primary DI / UDI-DI: EFIAN012050CUS1 FDA UDI
510(k) Number: K151156 FDA UDI
K163209 FDA UDI
FDA Product Code: HAW FDA UDI
GMDN Term: Multi-purpose stereotactic surgery system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 882.4560 FDA UDI
Commercial Distribution: Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

MRI Safety

MR Unsafe FDA UDI

BiopsyPointer 190 by Fiagon GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K151156 also covers:

FlexPointer 1.5 Cranial — Fiagon GmbH

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 II	Pending data

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Manufacturer

Manufacturer: Fiagon GmbH

Sources (1)

FDA UDI 53361710-4562-4aaa-94d0-ecda781f6043 37 fields · synced May 30, 2026