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Appasamy

EUDAMED

Class I (EU MDR)

Ref AA 2040

by Appasamy Associates Private Limited

Identity

Trade Name
Appasamy EUDAMED
Device Name
OPHTHALMIC SHARP INSTRUMENTS (EXCLUDING SCISSORS), REUSABLE EUDAMED
Model / Reference
AA 2040 EUDAMED

Identifiers

Primary DI / UDI-DI
08904343711444 EUDAMED
Basic UDI-DI
89043437MSI/SHARPPA EUDAMED
EMDN Code
L170401,L170402,L170499 EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Ireland 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

Appasamy by Appasamy Associates Private Limited — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
IN-MF-000012093
Authorised Representative
Amstermed B.V. NL-AR-000001971

Sources (1)

  • EUDAMED e67cc670-91a4-4707-9827-fba4dc2561df 61 fields · synced Jun 19, 2026