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ProxiDiagnost N90

FDA UDI

Class II (US FDA UDI)

by Philips Medical Systems GmbH, Dmc

Identity

Trade Name
ProxiDiagnost N90 FDA UDI
Generic Name
Stationary general-purpose fluoroscopic x-ray system, digital FDA UDI
Device Name
Image-intensified fluoroscopic x-ray system FDA UDI
Model / Reference
706100 FDA UDI
Description
Image-intensified fluoroscopic x-ray system FDA UDI

Identifiers

Catalog Number
706100 FDA UDI
Primary DI / UDI-DI
00884838085619 FDA UDI
FDA Product Code
JAA FDA UDI
GMDN Term
Stationary general-purpose fluoroscopic x-ray system, digital FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1650 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 general-purpose fluoroscopic x-ray system, digital

ProxiDiagnost N90 by Philips Medical Systems GmbH, Dmc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stationary general-purpose fluoroscopic x-ray system, digital.

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 86b3d965-bae0-4263-be64-5335000cf65a 35 fields · synced Jun 1, 2026