← Back to catalogue

IntelliVue XDS Software

FDA UDI

Class II (US FDA UDI)

by Philips Medizin Systeme Böblingen GmbH

Identity

Trade Name
IntelliVue XDS Software FDA UDI
Generic Name
Bedside information system application software FDA UDI
Device Name
IntelliVue XDS Software FDA UDI
Model / Reference
IntelliVue XDS Software FDA UDI
Description
IntelliVue XDS Software FDA UDI

Identifiers

Catalog Number
867019 FDA UDI
Primary DI / UDI-DI
00884838059313 FDA UDI
FDA Product Code
MSX FDA UDI
DSH FDA UDI
NSX FDA UDI
OUG FDA UDI
GMDN Term
Bedside information system application software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2300 FDA UDI
870.2800 FDA UDI
880.6310 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

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Bedside information system application software

IntelliVue XDS Software by Philips Medizin Systeme Böblingen GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bedside information system application software.

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 Medizin Systeme Böblingen GmbH

Sources (1)

  • FDA UDI 5621b589-f679-48d8-bb53-cf69862229c6 35 fields · synced Jun 6, 2026