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Reagiergefäß 2ml, PP, 75/Btl.

by SARSTEDT AG & Co.KG

Ref 72.708.007

Active European Union

CE IVDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 8 Nov 2026. What this means

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number4038917SARTD01901U74 Basic UDI-DI 04038917231374UDI-DIDate24 Jun 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Active

Specification

EUDAMED

Device name
Unp. Reagiergefäße (unsteril)
Model / reference
72.708.007
Primary DI / UDI-DI
04038917231374
Basic UDI-DI
4038917SARTD01901U74
Unit of use DI
04038917231381
EMDN code
W050301020202 Samples analyses, plastic microtubes without additives
Device class
Class A
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005649

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Properties

Other properties (13)

  • Supplied sterile: No
  • Sterilise before use: No
  • Contains human tissues or cells: No
  • Contains animal tissues or cells: No
  • Contains substances of microbial origin: No
  • Reagent: No
  • IVD kit: No
  • Self-testing: No
  • Near-patient testing: No
  • Professional testing: No
  • Companion diagnostics: No
  • IVD instrument: No
  • New device: No