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Pcr Eleva

FDA UDI

Class II (US FDA UDI)

by Philips Medical Systems GmbH, Dmc

Identity

Trade Name
PCR ELEVA FDA UDI
Generic Name
Computed radiography digital imaging scanner FDA UDI
Device Name
System Image Processing, Radiological FDA UDI
Model / Reference
9890-010-83731 FDA UDI
Description
System Image Processing, Radiological FDA UDI

Identifiers

Catalog Number
732050 FDA UDI
Primary DI / UDI-DI
00884838004047 FDA UDI
FDA Product Code
LLZ FDA UDI
GMDN Term
Computed radiography digital imaging scanner FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.2050 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: Computed radiography digital imaging scanner

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

Similar devices

Also classified as Computed radiography digital imaging scanner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9e009d17-e903-4515-813f-ccc4653b8f4e 34 fields · synced May 30, 2026