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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 UDIClass I (US FDA UDI)
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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Agilent Technologies Singapore Pte Ltd
Sources (1)
- FDA UDI 476c5716-37f7-459f-9e3d-c6f4c2d53f3b 37 fields · synced May 30, 2026