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Precision CRF

FDA UDI

Class II (US FDA UDI)

by Philips Medical Systems GmbH, Dmc

Identity

Trade Name
Precision CRF FDA UDI
Generic Name
Stationary general-purpose fluoroscopic x-ray system, digital FDA UDI
Device Name
The Precision CRF is a multi-functional general Radiography/ Fluoroscopy (R/F) system and includes • Footrest • Hand Grips Radiation Protection Accessories • Flexible Radiation Protection Apron • Front Radiation Protection Apron Additional Accessories (Optional) • Monitor Trolley • Monitor Ceiling Suspension • Parking Frame for Accessories • Shoulder Support • Side bar • Compression Belt • Adjustable Lateral Cassette Holder • Leg Supports • Infusion Bottle Holder • Arm Support for Catheterization • Ankle Clamps • Overhead Hand Grip • Adult Headrest • Mattress • Rotatable Stool for Footrest • Pediatric Micturition Set • Stretch Grip for Wall Stand • Bar Code Scanner • Patient Support • Stitching Ruler Accessories for the SkyPlate Detector (Optional) • Mobile Detector Holder • Detector Holder Patient Bed • Portable Panel Protector • Detector Handle • WPD Bags • Grids for SkyPlate Detector large FDA UDI
Model / Reference
706400 FDA UDI
Description
The Precision CRF is a multi-functional general Radiography/ Fluoroscopy (R/F) system and includes • Footrest • Hand Grips Radiation Protection Accessories • Flexible Radiation Protection Apron • Front Radiation Protection Apron Additional Accessories (Optional) • Monitor Trolley • Monitor Ceiling Suspension • Parking Frame for Accessories • Shoulder Support • Side bar • Compression Belt • Adjustable Lateral Cassette Holder • Leg Supports • Infusion Bottle Holder • Arm Support for Catheterization • Ankle Clamps • Overhead Hand Grip • Adult Headrest • Mattress • Rotatable Stool for Footrest • Pediatric Micturition Set • Stretch Grip for Wall Stand • Bar Code Scanner • Patient Support • Stitching Ruler Accessories for the SkyPlate Detector (Optional) • Mobile Detector Holder • Detector Holder Patient Bed • Portable Panel Protector • Detector Handle • WPD Bags • Grids for SkyPlate Detector large FDA UDI

Identifiers

Primary DI / UDI-DI
00884838110588 FDA UDI
FDA Product Code
JAA FDA UDI
KPR 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
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

No

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

Yes

FDA UDI

Category: Stationary general-purpose fluoroscopic x-ray system, digital

Precision CRF 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 29f5f9be-bc4e-4786-8516-15c31bac91d4 33 fields · synced May 30, 2026