Wireless digital flat panel detector

FDA UDI

Class II (US FDA UDI)

by iRay Group

Identity

Trade Name: Wireless digital flat panel detector FDA UDI
Generic Name: Indirect flat panel x-ray detector FDA UDI
Model / Reference: Mars1012V FDA UDI

Identifiers

Primary DI / UDI-DI: 06972093830052 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Indirect flat panel x-ray detector

Wireless digital flat panel detector by iRay Group — 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: iRay Group

Sources (1)

FDA UDI 5b5a26f5-956a-431a-98d6-e3ea735e5361 32 fields · synced Jun 8, 2026