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1717wce

FDA UDI

Class II (US FDA UDI)

by Rayence Co., Ltd.

Identity

Trade Name
1717WCE FDA UDI
Generic Name
Indirect flat panel x-ray detector FDA UDI
Device Name
Solid state x-ray imager (flat panel/digital imager) FDA UDI
Model / Reference
1717WCE FDA UDI
Description
Solid state x-ray imager (flat panel/digital imager) FDA UDI

Identifiers

Primary DI / UDI-DI
08800018602218 FDA UDI
510(k) Number
K242394 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

1717wce 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.

Cleared under the same submission

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 99393cd5-e1cb-4043-9b89-0ff1bc45a824 34 fields · synced May 30, 2026