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JW-i5000

by JW Pharmaceutical Corporation South Korea EUDAMED

Ref JW-i5000

EMDN Z1208040301

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number88093076112528J Basic UDI-DIDate29 Jan 2024RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Model / Reference
JW-i5000
Primary DI / UDI-DI
08809307611252
Basic UDI-DI
88093076112528J
EMDN Code
Z1208040301 Fixed neonatal incubators
Device Class
Class IIb
Market of Registration
Netherlands

Manufacturer details

EUDAMED SRN
KR-MF-000030307
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Other devices from JW Pharmaceutical Corporation

See all devices from JW Pharmaceutical Corporation →

Properties & raw data

Show properties, registry sources and raw records
  • Measuring Function
Other properties (12)
  • 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
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED c0e3875b-9383-4277-a146-8abb6fa9b008 61 fields · synced 22 Oct 2026