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Ms X-Ray Grid

FDA UDI

Class I (US FDA UDI)

by Mitaya Manufacturing Co., Ltd.

Identity

Trade Name
MS X-RAY GRID FDA UDI
Generic Name
Stationary x-ray grid FDA UDI
Device Name
PN:A2400TG, 475x475, 12:1, 110cm, 70L/cm FDA UDI
Model / Reference
GMSBK12110070S002 FDA UDI
Description
PN:A2400TG, 475x475, 12:1, 110cm, 70L/cm FDA UDI

Identifiers

Primary DI / UDI-DI
04589744212666 FDA UDI
FDA Product Code
IXJ FDA UDI
GMDN Term
Stationary x-ray grid FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.1910 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

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Stationary x-ray grid

Ms X-Ray Grid by Mitaya Manufacturing Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stationary x-ray grid.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ee629d13-13c4-4bbe-bca2-e506aa17ff74 33 fields · synced May 31, 2026