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CALCIUM (Ca)

FDA UDI

Class II (US FDA UDI)

by Randox Laboratories, Ltd.

Identity

Trade Name
CALCIUM (Ca) FDA UDI
Generic Name
Calcium (Ca2+) IVD, kit, spectrophotometry FDA UDI
Model / Reference
CA8309 FDA UDI

Identifiers

Primary DI / UDI-DI
05055273208368 FDA UDI
FDA Product Code
CJY FDA UDI
GMDN Term
Calcium (Ca2+) IVD, kit, spectrophotometry FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1145 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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 (Ca2+) IVD, kit, spectrophotometry

CALCIUM (Ca) by Randox Laboratories, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Calcium (Ca2+) IVD, kit, spectrophotometry.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b0585049-4294-4122-bdba-7e1f96401beb 32 fields · synced May 30, 2026