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PeriSafe

EUDAMED

Class IIa (EU MDR)

Ref 910200

by Peripal AG

Identity

Trade Name
PeriSafe EUDAMED
Device Name
PeriSafe EUDAMED
Model / Reference
910200 EUDAMED

Identifiers

Primary DI / UDI-DI
07640182580063 EUDAMED
Basic UDI-DI
764018258910200LE EUDAMED
B-07640182580063 EUDAMED
EMDN Code
F900199 PERITONAEAL DIALYSIS - OTHER EUDAMED

Classification

Device Class
Class IIa 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

PeriSafe by Peripal AG — Class IIa — MDD, MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Peripal AG
EUDAMED SRN
CH-MF-000011785
Authorised Representative
MED-RAS GmbH Regulatory Affairs Service DE-AR-000006211

Sources (2)

  • EUDAMED e046b0ec-2182-49fc-a1cf-afedcd024e6c 61 fields · synced Jun 19, 2026
  • EUDAMED ed49c768-4e78-4fcb-b94e-a523192e8c55 61 fields · synced May 19, 2026