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Patient BE

EUDAMED

Class I (EU MDR)

Ref 990587Model 3703

by Ivf Hartmann Ag

Identity

Trade Name
Patient BE EUDAMED
Device Name
Garment Sets non-sterile EUDAMED
Model / Reference
3703 EUDAMED
990587 EUDAMED

Identifiers

Primary DI / UDI-DI
07611600997114 EUDAMED
Basic UDI-DI
76116003703MV EUDAMED
EMDN Code
V0599 CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Medical Purpose
Single use, non-sterile procedure pack used to prepare the patient’s body for medical interventions and protection of the patient environment. EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Category: Ophthalmic surgical procedure kit, non-medicated, single-use

Patient BE by Ivf Hartmann Ag — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic surgical procedure kit, non-medicated, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Ivf Hartmann Ag
EUDAMED SRN
CH-PR-000019926

Sources (1)

  • EUDAMED bb6be4e8-d66f-430d-904d-55ec30f372de 61 fields · synced Oct 6, 2026