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Patient kit M

EUDAMED

Class I (EU MDR)

Ref 990537Model 3703

by Ivf Hartmann Ag

Identity

Trade Name
Patient kit M EUDAMED
Device Name
Garment Sets non-sterile EUDAMED
Model / Reference
3703 EUDAMED
990537 EUDAMED

Identifiers

Primary DI / UDI-DI
07611600995417 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

Patient kit M by Ivf Hartmann Ag — 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

Manufacturer
Ivf Hartmann Ag
EUDAMED SRN
CH-PR-000019926

Sources (1)

  • EUDAMED 31d005f5-01dd-42a6-b85c-433e868d529f 61 fields · synced Oct 6, 2026