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Percussion Wrap

by Seoil Pacific Corp.

Ref CV-100125, LModel CV-100125 L, CV-100124 M, CV-100123 S, CV-100122 XS

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number951701PercussionWrapMC Basic UDI-DI 08809517011804UDI-DIDate12 Oct 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Percussion Wrap
Model / Reference
CV-100125 L, CV-100124 M, CV-100123 S, CV-100122 XS, CV-100125, L
Primary DI / UDI-DI
08809517011804
Basic UDI-DI
951701PercussionWrapMC
EMDN Code
V0880 Medical support equipment - accessories
Device Class
Class IIa
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
KR-MF-000012478
Authorised representative
Advena Limited MT-AR-000000234

Other devices from Seoil Pacific Corp.

See all devices from Seoil Pacific Corp. →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No