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Semi-automatic Biopsy-Needle BIM 16/15

FDA UDI

Class II (US FDA UDI)

by ITP Innovative Tomography Products GmbH

Identity

Trade Name
Semi-automatic Biopsy-Needle BIM 16/15 FDA UDI
Generic Name
End-cut biopsy gun handpiece/needle FDA UDI
Device Name
The biopsy-needle is intended for soft-tissue biopsy (such as breast, kidney, liver, prostate). FDA UDI
Model / Reference
BIM 16/15 FDA UDI
Description
The biopsy-needle is intended for soft-tissue biopsy (such as breast, kidney, liver, prostate). FDA UDI

Identifiers

Primary DI / UDI-DI
04262410685086 FDA UDI
FDA Product Code
KNW FDA UDI
GMDN Term
End-cut biopsy gun handpiece/needle FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1075 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Length — 150 Millimeter FDA UDI
Needle Gauge — 16 Gauge FDA UDI

Category: End-cut biopsy gun handpiece/needle

Semi-automatic Biopsy-Needle BIM 16/15 by ITP Innovative Tomography Products GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as End-cut biopsy gun handpiece/needle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3a119524-0247-40b2-a773-b7a4d5b6dfe0 36 fields · synced May 30, 2026