← Back to catalogue

PodoPlasma

EUDAMED

Class I (EU MDR)

Ref PC100007

by terraplasma medical GmbH

Identity

Trade Name
PodoPlasma EUDAMED
Device Name
plasma derma care EUDAMED
Model / Reference
PC100007 EUDAMED

Identifiers

Primary DI / UDI-DI
04260644540133 EUDAMED
Basic UDI-DI
426064454PDCFZ EUDAMED
Direct Marketing DI
04260644540133 EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

Category: Device sterilization/disinfection container, reusable

PodoPlasma by terraplasma medical GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
DE-MF-000011250

Sources (1)

  • EUDAMED a8f06e64-5676-4962-bb30-4c1090082ecb 61 fields · synced Jul 21, 2026