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IntelliSpace Cardiovascular

FDA UDI

Class II (US FDA UDI)

by Philips Medical Systems Nederland B.V.

Identity

Trade Name
IntelliSpace Cardiovascular FDA UDI
Generic Name
Radiology picture archiving and communication system workstation FDA UDI
Device Name
Cardiovascular Image and Information Management Solution (CVIS) FDA UDI
Model / Reference
IntelliSpace Cardiovascular 2.2 FDA UDI
Description
Cardiovascular Image and Information Management Solution (CVIS) FDA UDI

Identifiers

Catalog Number
98960612323X FDA UDI
Primary DI / UDI-DI
00884838085220 FDA UDI
510(k) Number
K153022 FDA UDI
FDA Product Code
LLZ FDA UDI
GMDN Term
Radiology picture archiving and communication system workstation 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

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Radiology picture archiving and communication system workstation

IntelliSpace Cardiovascular by Philips Medical Systems Nederland B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiology picture archiving and communication system workstation.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 496c21c0-1132-476c-a48b-7769d71aa5fb 36 fields · synced Sep 18, 2026