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Anti-scatter Grid (40/8/180) - OEM

FDA UDI

Class I (US FDA UDI)

by Philips Medical Systems GmbH, Dmc

Identity

Trade Name
Anti-scatter Grid (40/8/180) - OEM FDA UDI
Generic Name
Stationary x-ray grid FDA UDI
Device Name
Accessory for GE system FDA UDI
Model / Reference
9896-010-74401 FDA UDI
Description
Accessory for GE system FDA UDI

Identifiers

Primary DI / UDI-DI
00884838110007 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

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Stationary x-ray grid

Anti-scatter Grid (40/8/180) - OEM by Philips Medical Systems GmbH, Dmc — 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 2c928f22-bb31-4678-bc94-60c6c1038c60 33 fields · synced Jun 6, 2026