Identity
- Trade Name
- Brand name FDA UDI
- Generic Name
- General-purpose centrifuge IVD FDA UDI
- Device Name
- Di Description FDA UDI
- Model / Reference
- A40400 FDA UDI
- Description
- Di Description FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10859952006014 FDA UDI
- FDA Product Code
- GGK FDA UDIOZE FDA UDIJJX FDA UDI
- GMDN Term
- General-purpose centrifuge IVD FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.8540 FDA UDI866.3980 FDA UDI862.1660 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
Yes
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dry Heat Sterilization FDA UDI
Brand name by Life Technologies Limited — 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
- Life Technologies Limited
Sources (1)
- FDA UDI 36f29ddc-1b21-4dce-9718-5f0e0bb4ee89 34 fields · synced May 30, 2026