Identity
- Trade Name
- Boost 4+ Flex Centrifuge, Dr. PRP FDA UDI
- Generic Name
- General-purpose centrifuge IVD FDA UDI
- Device Name
- General purpose laboratory centrifuge for sample separation. FDA UDI
- Model / Reference
- 00-389-102-002 FDA UDI
- Description
- General purpose laboratory centrifuge for sample separation. FDA UDI
Identifiers
- Catalog Number
- 00-389-102-002 FDA UDI
- Primary DI / UDI-DI
- 00810052863573 FDA UDI
- FDA Product Code
- JQC FDA UDI
- GMDN Term
- General-purpose centrifuge IVD FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.2050 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Boost 4+ Flex Centrifuge, Dr. PRP by Drucker Diagnostics — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Drucker Diagnostics
Sources (1)
- FDA UDI 8ea66ecc-e77c-4283-93ca-7fa2e2fafdb4 35 fields · synced Jun 6, 2026