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aZure Drill Extension

EUDAMED

Class IIa (EU MDR)

Ref DI0SK00001Model DrillModel Drill Extension

by INTAI Technology Corp.

Identity

Trade Name
aZure Drill Extension EUDAMED
Device Name
Drill EUDAMED
Drill Extension EUDAMED
Model / Reference
Drill EUDAMED
DI0SK00001 EUDAMED
Drill Extension EUDAMED

Identifiers

Primary DI / UDI-DI
04719874672324 EUDAMED
Basic UDI-DI
471987675DR0001F6 EUDAMED
B-04719874672324 EUDAMED
EMDN Code
L99 SURGICAL INSTRUMENTS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMED

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

Category: Surgical retraction system, reusable

aZure Drill Extension by INTAI Technology Corp. — Class IIa — MDD, MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retraction system, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
TW-MF-000001158
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (2)

  • EUDAMED 2d47ca9b-0377-4139-b4ff-038ba9c4efba 61 fields · synced Jul 18, 2026
  • EUDAMED 02131418-9f48-40ac-a7c5-8e21c93503cf 61 fields · synced May 17, 2026