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Atellica CH Cocaine (CocC) 11701328

by Siemens Healthcare Diagnostics Inc.

Ref 11701328Model IVDR_67_TTN_DUB-C_B_REAG_Cocaine Metabolite

Active European Union. Also listed in GUDID (US).

CE IVDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

None found

in data synced 24 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

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 Number0405686901687WE Basic UDI-DI 00630414654195UDI-DIDate9 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00630414654195 UDI-DI Date15 Oct 2025ListedStatusListed GUDID: in commercial distribution

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.

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 24 Oct 2026.

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  • Withdrawn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
Atellica CH Cocaine (CocC)
Generic Name
Cocaine/cocaine metabolite IVD, kit, enzyme immunoassay (EIA),
Device Name
IVDR_67_TTN_DUB-C_B_REAG_Cocaine Metabolite
Model / Ref / Catalog
11701328, IVDR_67_TTN_DUB-C_B_REAG_Cocaine Metabolite
Primary DI / UDI-DI
00630414654195
Basic UDI-DI
0405686901687WE
Unit of Use DI
00630414321967
510(k) Number
FDA Product Code
DIO
EMDN Code
W0102090106 Cocaine + cocaine metabolites
GMDN Term
Cocaine/cocaine metabolite IVD, kit, enzyme immunoassay (EIA),
Device Class
Class B EUDAMED
Class II GUDID
Regulation Number
862.3250
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class B
GUDID
Class II

Related devices

Cleared under the same submission (K031512)

Other devices from Siemens Healthcare Diagnostics Inc.

See all devices from Siemens Healthcare Diagnostics Inc. →

Properties

  • Animal Tissues
  • Microbial Substances
  • Reagent
  • Professional Testing
  • Lot / Batch Number
  • Expiration Date

Other properties (18)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Human Tissues: No
  • Self Testing: No
  • Near-Patient 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
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No