Identity
- Trade Name
- 2430TCA FDA UDI
- Generic Name
- Indirect flat panel x-ray detector FDA UDI
- Device Name
- Full-Field Digital Mammography System FDA UDI
- Model / Reference
- 2430TCA FDA UDI
- Description
- Full-Field Digital Mammography System FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08800018602256 FDA UDI
- 510(k) Number
- K243849 FDA UDI
- FDA Product Code
- MUE FDA UDILLZ FDA UDI
- GMDN Term
- Indirect flat panel x-ray detector FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1715 FDA UDI892.2050 FDA UDI
- Commercial Distribution
- 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
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Indirect flat panel x-ray detector
2430tca by Rayence Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Rayence Co., Ltd.
Sources (1)
- FDA UDI 14327f9d-3a03-456e-803b-2c1d6dac4726 34 fields · synced May 30, 2026