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Multivette® 600 LH 15.1673.100

by Sarstedt Aktiengesellschaft & Co.KG

Ref 15.1673.100

Active European Union. Also listed in GUDID (US), not in commercial distribution.

CE IVDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

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

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR EUDAMED Number4038917SARTD00700U68 Basic UDI-DI 04038917132992UDI-DIDate13 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04038917132992 UDI-DI Date30 Nov 2022ListedStatusListed GUDID: not in commercial distribution

Certificates

0 certificates · EUDAMED

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

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/IVDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Multivette® 600 LH
Generic Name
Capillary blood transfer tube IVD, heparin
Device Name
Multivette®
Model / Ref / Catalog
15.1673.100
Primary DI / UDI-DI
04038917132992
Basic UDI-DI
4038917SARTD00700U68
Unit of Use DI
04038917205214
FDA Product Code
GIO
EMDN Code
W050101010201 Blood collection, tubes with additives or serum separator
GMDN Term
Capillary blood transfer tube IVD, heparin
Device Class
Class A EUDAMED
Class I GUDID
Regulation Number
864.6150
EU market of registration
Germany
GUDID distribution status
Not in Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class A
GUDID
Class I

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Properties

  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (20)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Professional Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No