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Calcium Chloride Solution 10873872

by Siemens Healthcare Diagnostics Products Ltd

Ref 10873872Model IVDR_27_MAR EB_A_PROF_REAG_CaCl2

Calcium Chloride Solution 10873872 is a device classified as Class A in the EU and Class II in the US made by Siemens Healthcare Diagnostics Products Ltd, registered in EUDAMED on 12 Jun 2026 (Basic UDI-DI 0405686900157V5), cleared under FDA 510(k) K924509 on 21 Dec 1992 and listed in FDA GUDID since 25 Mar 2024 (UDI-DI 00630414640563), active as of 25 Oct 2026.

Active European Union and United States. Also listed in GUDID (US).

CE IVDR 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 25 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K924509

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR EUDAMED Number0405686900157V5 Basic UDI-DI 00630414640563UDI-DIDate12 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00630414640563 UDI-DI Date25 Mar 2024ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK924509 Date21 Dec 1992DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI 0405686900157V5 registered 12 Jun 2026 Active
  • FDA 510(k) K924509 decided 21 Dec 1992 Active
  • FDA GUDID UDI-DI 00630414640563 listed 25 Mar 2024 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K924509
  2. Listed FDA GUDID 00630414640563
  3. Registered EUDAMED 0405686900157V5

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/IVDR Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
Calcium Chloride Solution
Generic name
Calcium chloride coagulation reagent IVD
Device name
IVDR_27_MAR EB_A_PROF_REAG_CaCl2
Model / Ref / Catalog
10873872, IVDR_27_MAR EB_A_PROF_REAG_CaCl2
Primary DI / UDI-DI
00630414640563
Basic UDI-DI
0405686900157V5
Unit of use DI
00842768018916
510(k) Number
FDA product code
JPA
EMDN code
W0103020901 Calcium chloride
GMDN term
Calcium chloride coagulation reagent IVD
Device class
Class A EUDAMED
Class II GUDID
Regulation number
864.5425
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class A
GUDID
Class II

Device class is stated on each registry's own scale: Class A in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Calcium chloride coagulation reagent IVD

Cleared under the same submission (K924509)

Similar devices in this category

Other devices filed under AUXILIARY REAGENTS AND SUPPLEMENTS (HAEMOSTASIS).

Other devices from Siemens Healthcare Diagnostics Products Ltd

See all devices from Siemens Healthcare Diagnostics Products Ltd →

Properties

  • Reagent
  • Professional testing
  • Lot / batch number
  • Expiration date
Other properties (22, all answered No)