← Back to catalogue

Bonopty Extended Drill 13G, 16.5 cm

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 12-1274

by AprioMed AB

Identity

Trade Name
Bonopty Extended Drill 13G, 16.5 cm EUDAMED
Bonopty Extended Drill FDA UDI
Generic Name
Bone biopsy needle FDA UDI
Device Name
Bonopty EUDAMED
Extended drill that can be used together with AprioMed Bonopty Penetration Set 12G. FDA UDI
Model / Reference
12-1274 EUDAMED
G032 FDA UDI
Description
Extended drill that can be used together with AprioMed Bonopty Penetration Set 12G. FDA UDI

Identifiers

Catalog Number
12-1274 FDA UDI
Primary DI / UDI-DI
07350031350326 EUDAMEDFDA UDI
Basic UDI-DI
73500313511KG EUDAMED
FDA Product Code
GAA FDA UDI
EMDN Code
A0102010101 SHEARING BIOPSY NEEDLES EUDAMED
GMDN Term
Bone biopsy needle FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Market of Registration
Sweden EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 2.45 Millimeter FDA UDI
Length — 16.5 Centimeter FDA UDI

Bonopty Extended Drill 13G, 16.5 cm by Apriomed AB — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
AprioMed AB
EUDAMED SRN
SE-MF-000001013

Sources (2)

  • EUDAMED b40db52e-0974-4ade-ba87-df735259ab26 61 fields · synced Jun 18, 2026
  • FDA UDI bb2512d6-81c7-47dc-9bb0-2a21da713435 36 fields · synced May 30, 2026