Sr-130-G

FDA UDI

Class II (US FDA UDI)

by Source-Ray, Inc.

Identity

Trade Name: SR-130-G FDA UDI
Generic Name: Diagnostic x-ray system generator, mobile FDA UDI
Device Name: X-Ray Generator / Tube Housing Assembly, 100kVp / 30mA FDA UDI
Model / Reference: SR-130-G FDA UDI
Description: X-Ray Generator / Tube Housing Assembly, 100kVp / 30mA FDA UDI

Identifiers

Catalog Number: 910056 FDA UDI
Primary DI / UDI-DI: 00868162000241 FDA UDI
510(k) Number: K030494 FDA UDI
FDA Product Code: IZL FDA UDI
GMDN Term: Diagnostic x-ray system generator, mobile FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 892.1720 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

Yes

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

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Diagnostic x-ray system generator, mobile

Sr-130-G by Source-Ray, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K030494 also covers:

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: Source-Ray, Inc.

Sources (1)

FDA UDI f4c8e06b-8b70-434f-884a-649a9ce79e98 36 fields · synced May 30, 2026