← Back to catalogue

DigitalDiagnost

FDA UDI

Class II (US FDA UDI)

by Philips Medical Systems GmbH, Dmc

Identity

Trade Name
DigitalDiagnost FDA UDI
Generic Name
Stationary basic diagnostic x-ray system, digital FDA UDI
Device Name
Solid State X-Ray Imager (Flat Panel/Digital Imager) FDA UDI
Model / Reference
712226 FDA UDI
Description
Solid State X-Ray Imager (Flat Panel/Digital Imager) FDA UDI

Identifiers

Catalog Number
712226 FDA UDI
Primary DI / UDI-DI
00884838085671 FDA UDI
FDA Product Code
MQB FDA UDI
GMDN Term
Stationary basic diagnostic x-ray system, digital FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1680 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

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

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 basic diagnostic x-ray system, digital

DigitalDiagnost by Philips Medical Systems GmbH, Dmc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stationary basic diagnostic x-ray system, digital.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Philips Medical Systems GmbH, Dmc

Sources (1)

  • FDA UDI b0857454-7e17-491e-901a-7693ecbb79a7 34 fields · synced May 30, 2026