← Back to catalogue

Drill Bit Ø1.9 mm × 175 mm

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref B-410015 Model Bonebridge Instrument-IIa

by Bonebridge AG

Identity

Trade Name
Drill Bit Ø1.9 mm × 175 mm EUDAMED
Drill Bit Ø1.9mm x 175mm FDA UDI
Generic Name
Fluted surgical drill bit, reusable FDA UDI
Device Name
Bonebridge Instrument-IIa EUDAMED
Model / Reference
Bonebridge Instrument-IIa EUDAMED
B-410015 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
07640187462920 EUDAMEDFDA UDI
Basic UDI-DI
764018746InstrumentsIIa9G EUDAMED
Direct Marketing DI
07640187462920 EUDAMED
FDA Product Code
HTW FDA UDI
EMDN Code
L091001 INSTRUMENTS FOR INSERTION AND EXTRACTION OF MATERIALS FOR OSTEOSYNTHESIS, REUSABLE EUDAMED
GMDN Term
Fluted surgical drill bit, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Drill Bit Ø1.9 mm × 175 mm by Bonebridge AG — 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
Bonebridge AG
EUDAMED SRN
CH-MF-000013933
Authorised Representative
Axxos GmbH DE-AR-000005590

Sources (3)

  • EUDAMED 99187881-8b44-497c-8c88-dfdef59300fa 61 fields · synced Jul 24, 2026
  • FDA UDI 7d3c4e0b-9867-48a5-8435-4b340bb8904a 32 fields · synced May 29, 2026
  • EUDAMED 1dfb214a-30c9-42c8-b120-a3fa281e60ca 61 fields · synced Jul 24, 2026