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1417wcc

FDA UDI

Class II (US FDA UDI)

by Rayence Co., Ltd.

Identity

Trade Name
1417WCC FDA UDI
Generic Name
Indirect flat panel x-ray detector FDA UDI
Device Name
1417WCC is a digital X-ray flat panel detector that can acquire radiographic images of human anatomy when used with existing radiographic x-ray systems FDA UDI
Model / Reference
1417WCC FDA UDI
Description
1417WCC is a digital X-ray flat panel detector that can acquire radiographic images of human anatomy when used with existing radiographic x-ray systems FDA UDI

Identifiers

Primary DI / UDI-DI
08800018600559 FDA UDI
510(k) Number
K171418 FDA UDI
FDA Product Code
MQB FDA UDI
GMDN Term
Indirect flat panel x-ray detector FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1680 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

1417wcc 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 ff820b32-51f7-460f-a8d2-52b8b8979399 35 fields · synced May 31, 2026