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Kappa (M) + Lambda (P)

FDA UDI

Class I (US FDA UDI)

by Biocare Medical, Llc

Identity

Trade Name
Kappa (M) + Lambda (P) FDA UDI
Generic Name
Kappa/lambda light chain immunoglobulin IVD, antibody FDA UDI
Model / Reference
API3159DSAA FDA UDI

Identifiers

Primary DI / UDI-DI
00847627004451 FDA UDI
FDA Product Code
NJT FDA UDI
GMDN Term
Kappa/lambda light chain immunoglobulin IVD, antibody FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.1860 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

Yes

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

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: Kappa/lambda light chain immunoglobulin IVD, antibody

Kappa (M) + Lambda (P) by Biocare Medical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Kappa/lambda light chain immunoglobulin IVD, antibody.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bd2873a9-0ec1-49ca-aa27-1a87b28b1898 33 fields · synced May 30, 2026