Identity
- Trade Name
- LT Medical Centrifuge for PRP FDA UDI
- Generic Name
- Haematological concentrate system centrifuge FDA UDI
- Model / Reference
- LTA-3000 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06974621793389 FDA UDI
- FDA Product Code
- JQC FDA UDI
- GMDN Term
- Haematological concentrate system centrifuge 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
LT Medical Centrifuge for PRP by Zhuhai Longtime Biological Technology Co., Ltd — 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
- Zhuhai Longtime Biological Technology Co., Ltd
Sources (1)
- FDA UDI ac0a3358-3807-4669-9b92-4a9923494e89 33 fields · synced May 30, 2026