← Back to catalogue

Anti-scatter Grid (60 +2 more)

FDA UDIEUDAMED

Class I (US FDA UDI)

by Philips Medical Systems GmbH, Dmc

Identity

Trade Name
Anti-scatter Grid (60/10/140) FDA UDI
Generic Name
Stationary x-ray grid FDA UDI
Model / Reference
9896-010-64292 FDA UDI

Identifiers

Primary DI / UDI-DI
00884838097322 FDA UDI
FDA Product Code
IXJ FDA UDI
GMDN Term
Stationary x-ray grid FDA UDI
Models / Variants
60 FDA UDIEUDAMED
10 FDA UDIEUDAMED
140 FDA UDIEUDAMED

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 (60 +2 more) by Philips Medical Systems GmbH, Dmc — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — 3 models

Similar devices

Also classified as Stationary x-ray grid.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (2)

  • FDA UDI ed06a293-6d8e-4f3a-a0e5-616f7ace6cdb 32 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 3, 2026