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MedTest DX Total Protein for the BS200
FDA UDIClass II (US FDA UDI)
by Medtest DX
Identity
- Trade Name
- MedTest DX Total Protein for the BS200 FDA UDI
- Generic Name
- Total protein IVD, reagent FDA UDI
- Device Name
- For the quantitative determination of total protein concentration in serum using the Mindray BS-200 analyzer. 3 x 40ml. FDA UDI
- Model / Reference
- TP600 FDA UDI
- Description
- For the quantitative determination of total protein concentration in serum using the Mindray BS-200 analyzer. 3 x 40ml. FDA UDI
Identifiers
- Catalog Number
- TP600 FDA UDI
- Primary DI / UDI-DI
- 00817439021304 FDA UDI
- FDA Product Code
- CEK FDA UDI
- GMDN Term
- Total protein IVD, reagent FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1635 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
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Conditional FDA UDI
MedTest DX Total Protein for the BS200 by Medtest DX — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 II | Pending data |
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Manufacturer
- Manufacturer
- Medtest DX
Sources (1)
- FDA UDI 78ca69e6-7a00-432e-8bf1-a09d453d601a 37 fields · synced Jun 8, 2026