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N-Acetyl-β-D-Glucosaminidase (NAG) Test Kit (MPT Method)

by URIT Medical Electronic Co., Ltd. EUDAMED

Active European Union

Ref "REF: U82182030M, U82189060M, U82185015M, U82111020M"

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-6-31A5 Basic UDI-DIDate21 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/IVDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
N-Acetyl-β-D-Glucosaminidase (NAG) Test Kit (MPT Method)
Model / Reference
"REF: U82182030M, U82189060M, U82185015M, U82111020M"
Primary DI / UDI-DI
D-6-31A5
Basic UDI-DI
B-6-31A5
EMDN Code
W01010126 N-acetyl-b, d-glucosaminidase
Device Class
Class IVD General
Market of Registration
Spain

Manufacturer details

EUDAMED SRN
CN-MF-000011840
Authorised representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

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See all devices from URIT Medical Electronic Co., Ltd. →

Properties

  • Microbial Substances
  • Reagent
  • Professional Testing

Other properties (7)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No