← Back to catalogue

Percuton

EUDAMED

Class IIa (EU MDR)

Ref PERCUTON

by BARK Technology Pte Ltd

Identity

Trade Name
PERCUTON EUDAMED
Device Name
Vibroacoustic device EUDAMED
Model / Reference
PERCUTON EUDAMED

Identifiers

Primary DI / UDI-DI
08881300587000 EUDAMED
Basic UDI-DI
8881300587PERCUTONJY EUDAMED
EMDN Code
Z120616 ELECTROMECHANICAL SYSTEMS FOR PHYSICAL THERAPY EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Portugal 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

Percuton by BARK Technology Pte Ltd — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

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
SG-MF-000030991
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 5ae218a6-5e03-47ba-9176-5671f72a1d97 61 fields · synced Jun 18, 2026