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Single-Use Endfire Biopsy Guide

FDA UDI

Class II (US FDA UDI)

by Bk Medical ApS

Identity

Trade Name
Single-Use Endfire Biopsy Guide FDA UDI
Generic Name
Needle guide, single-use FDA UDI
Device Name
Sterile-packed. Bore diameter 1.6 mm; angle of insertion 0° to the long axis of the transducer FDA UDI
Model / Reference
UA1323-S FDA UDI
Description
Sterile-packed. Bore diameter 1.6 mm; angle of insertion 0° to the long axis of the transducer FDA UDI

Identifiers

Primary DI / UDI-DI
05704916000769 FDA UDI
FDA Product Code
FCG FDA UDI
GMDN Term
Needle guide, single-use 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

Yes

FDA UDI

Category: Needle guide, single-use

Single-Use Endfire Biopsy Guide by Bk Medical ApS — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Needle guide, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bk Medical ApS

Sources (1)

  • FDA UDI 45c7864e-576b-4017-a63f-668b87183f60 34 fields · synced May 30, 2026