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Aseltech

EUDAMED

Class I (EU MDR)

Ref BP-1302Model ASELTECH

by Asel Tibbi Aletler A.S.

Identity

Trade Name
ASELTECH EUDAMED
Device Name
SCRAPER EUDAMED
Model / Reference
ASELTECH EUDAMED
BP-1302 EUDAMED

Identifiers

Primary DI / UDI-DI
08681376066375 EUDAMED
Basic UDI-DI
8681376ASELTECH201530AG EUDAMED
EMDN Code
L1703 OPHTHALMOLOGY CURETTES, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Türkiye 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: Ophthalmic curette, reusable

Aseltech by Asel Tibbi Aletler A.S. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic curette, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
TR-MF-000019723

Sources (1)

  • EUDAMED 467d6716-7212-4991-9214-16ae9c86e18b 61 fields · synced Jun 19, 2026