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2430tca

FDA UDI

Class II (US FDA UDI)

by Rayence Co., Ltd.

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 UDI
LLZ FDA UDI
GMDN Term
Indirect flat panel x-ray detector FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1715 FDA UDI
892.2050 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

Similar devices

Also classified as Indirect flat panel x-ray detector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Rayence Co., Ltd.

Sources (1)

  • FDA UDI 14327f9d-3a03-456e-803b-2c1d6dac4726 34 fields · synced May 30, 2026