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Calcium Chloride Solution

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics Products Ltd

Identity

Trade Name
Calcium Chloride Solution FDA UDI
Generic Name
Calcium chloride coagulation reagent IVD FDA UDI
Device Name
Supplementary Reagent for coagulation tests FDA UDI
Model / Reference
10873872 FDA UDI
Description
Supplementary Reagent for coagulation tests FDA UDI

Identifiers

Catalog Number
10873872 FDA UDI
Primary DI / UDI-DI
00630414640563 FDA UDI
510(k) Number
K924509 FDA UDI
FDA Product Code
JPA FDA UDI
GMDN Term
Calcium chloride coagulation reagent IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.5425 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Calcium chloride coagulation reagent IVD

Calcium Chloride Solution by Siemens Healthcare Diagnostics Products Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Calcium chloride coagulation reagent IVD.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6405e5d8-0626-4ae3-a2a2-869fcf4b04bb 37 fields · synced May 31, 2026