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Ms anti-Multidrug Resistance 1 (C494) Concentrate

FDA UDI

Class I (US FDA UDI)

by Life Technologies Limited

Identity

Trade Name
Ms anti-Multidrug Resistance 1 (C494) Concentrate FDA UDI
Generic Name
Multiple solid tumour differentiation marker IVD, kit, enzyme immunoassay (EIA) FDA UDI
Model / Reference
187243 FDA UDI

Identifiers

Primary DI / UDI-DI
10190302008129 FDA UDI
FDA Product Code
NJT FDA UDI
GMDN Term
Multiple solid tumour differentiation marker IVD, kit, enzyme immunoassay (EIA) 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: Multiple solid tumour differentiation marker IVD, kit, enzyme immunoassay (EIA)

Ms anti-Multidrug Resistance 1 (C494) Concentrate by Life Technologies Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple solid tumour differentiation marker IVD, kit, enzyme immunoassay (EIA).

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e3dae6cc-ca73-4216-8ae2-fc6d327d5a7e 32 fields · synced May 30, 2026