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Atellica CH LSP Calibrator 11099434

by Siemens Healthcare Diagnostics Inc.

Ref 11099434Model IVDR_67_TTN_DUB-C_B_REAG_LSP CAL

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 Number0405686901743VX Basic UDI-DI 00630414597553UDI-DIDate8 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00630414597553 UDI-DI Date27 Dec 2017ListedStatusListed 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  • Withdrawn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 Liquid Specific Protein Calibrators (LSP CAL) EUDAMED
Atellica CH LSP Calibrator GUDID
Generic Name
Multiple-type clinical chemistry analyte profile IVD, calibrator
Device Name
IVDR_67_TTN_DUB-C_b_reag_lsp Cal
Model / Ref / Catalog
11099434, IVDR_67_TTN_DUB-C_B_REAG_LSP CAL
Primary DI / UDI-DI
00630414597553
Basic UDI-DI
0405686901743VX
510(k) Number
FDA Product Code
JIX
EMDN Code
W0102152299 Standards and calibrators - immunochemistry - other
GMDN Term
Multiple-type clinical chemistry analyte profile IVD, calibrator
Device Class
Class B EUDAMED
Class II GUDID
Regulation Number
862.1150
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

Category: Multiple-type clinical chemistry analyte profile IVD, calibrator

Cleared under the same submission (K103701)

Other devices from Siemens Healthcare Diagnostics Inc.

See all devices from Siemens Healthcare Diagnostics Inc. →

Properties

  • Human Tissues
  • Reagent
  • Professional Testing
  • Lot / Batch Number
  • Expiration Date

Other properties (19)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Animal Tissues: No
  • Microbial Substances: 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