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Anti-scatter Grid (36 +2 more)

FDA UDI

Class I (US FDA UDI)

by Philips Medical Systems GmbH, Dmc

Identity

Trade Name
Anti-scatter Grid (36/12/100) FDA UDI
Generic Name
Stationary x-ray grid FDA UDI
Model / Reference
9896-010-61302 FDA UDI

Identifiers

Primary DI / UDI-DI
00884838097506 FDA UDI
FDA Product Code
IXJ FDA UDI
GMDN Term
Stationary x-ray grid FDA UDI
Models / Variants
36 FDA UDI
12 FDA UDI
100 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 (36 +2 more) by Philips Medical Systems GmbH, Dmc — Class I — FDA UDI — listed in FDA GUDID — 3 models — 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

Manufacturer
Philips Medical Systems GmbH, Dmc

Sources (1)

  • FDA UDI 60e80cbb-6960-45d1-950c-f34cf0ae578c 32 fields · synced May 30, 2026