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Patient Interface for SCHWIND ATOS

EUDAMED

Class I (EU MDR)

Ref 25132

by SCHWIND eye-tech-solutions GmbH

Identity

Trade Name
Patient Interface for SCHWIND ATOS EUDAMED
Device Name
Patient Interface for SCHWIND ATOS EUDAMED
Model / Reference
25132 EUDAMED

Identifiers

Primary DI / UDI-DI
04260157142336 EUDAMED
Basic UDI-DI
426015714E090-FEMTOPI4N EUDAMED
Unit of Use DI
04260157142329 EUDAMED
EMDN Code
Z12011085 LASER SURGERY INSTRUMENTS - CONSUMABLES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

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: Varicose vein lasing procedure kit

Patient Interface for SCHWIND ATOS by SCHWIND eye-tech-solutions GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Varicose vein lasing procedure kit.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
DE-MF-000019049

Sources (1)

  • EUDAMED ad6f856c-ecf5-4d03-80ea-aaed4d6233ae 61 fields · synced Jul 15, 2026