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Cryopen XP+

EUDAMED

Class IIa (EU MDR)

Ref S-HO-CEPEPLUS-00

by H&O Equipments nv/sa

Identity

Trade Name
Cryopen XP+ EUDAMED
Device Name
CryoPen EUDAMED
Model / Reference
S-HO-CEPEPLUS-00 EUDAMED

Identifiers

Primary DI / UDI-DI
15407008480520 EUDAMED
Basic UDI-DI
540700848SHOCPECLFP8G EUDAMED
Direct Marketing DI
15407008480520 EUDAMED
EMDN Code
Z120102 CRYOSURGERY EQUIPMENT EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

No

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

Cryopen XP+ by H&O Equipments nv/sa — Class IIa — 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
BE-MF-000000992

Sources (1)

  • EUDAMED 1b7d3033-a1ef-4aac-be84-5ac3f89a7e81 61 fields · synced Jun 18, 2026