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LIPOPROTEIN (a) (Lp (a))

FDA UDI

Class I (US FDA UDI)

by Randox Laboratories, Ltd.

Identity

Trade Name
LIPOPROTEIN (a) (Lp (a)) FDA UDI
Generic Name
Lipoprotein A IVD, kit, nephelometry/turbidimetry FDA UDI
Model / Reference
LP8324 FDA UDI

Identifiers

Primary DI / UDI-DI
05055273209235 FDA UDI
FDA Product Code
MSM FDA UDI
GMDN Term
Lipoprotein A IVD, kit, nephelometry/turbidimetry FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1475 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Lipoprotein A IVD, kit, nephelometry/turbidimetry

LIPOPROTEIN (a) (Lp (a)) by Randox Laboratories, Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Lipoprotein A IVD, kit, nephelometry/turbidimetry.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ca27afe6-2f11-4086-8fc9-0cd73673cefb 32 fields · synced May 30, 2026