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Mono Mo a Hu CD19/FITC + Poly Rb a Hu Lambda LC/RPE + Poly Rb a Hu Kappa LC/APC

FDA UDI

Class I (US FDA UDI)

by Agilent Technologies Singapore Pte Ltd

Identity

Trade Name
Mono Mo a Hu CD19/FITC + Poly Rb a Hu Lambda LC/RPE + Poly Rb a Hu Kappa LC/APC FDA UDI
Generic Name
Multiple CD cell marker IVD, antibody FDA UDI
Device Name
MultiMix Triple-Colour Reagent Anti-Human CD19/FITC Anti-Human Lambda Light Chains/RPE Anti-Human Kappa Light Chains/APC FDA UDI
Model / Reference
TC669 FDA UDI
Description
MultiMix Triple-Colour Reagent Anti-Human CD19/FITC Anti-Human Lambda Light Chains/RPE Anti-Human Kappa Light Chains/APC FDA UDI

Identifiers

Primary DI / UDI-DI
05700572020165 FDA UDI
FDA Product Code
MVU FDA UDI
GMDN Term
Multiple CD cell marker IVD, antibody FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.4020 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 1 Milliliter FDA UDI

Mono Mo a Hu CD19/FITC + Poly Rb a Hu Lambda LC/RPE + Poly Rb a Hu Kappa LC/APC by Agilent Technologies Singapore Pte Ltd — Class I — FDA UDI — listed in FDA…

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 476c5716-37f7-459f-9e3d-c6f4c2d53f3b 37 fields · synced May 30, 2026