CAAS IntraVascular

GUDID 08056304454065

Pie Medical Imaging B.V.

Radiology DICOM image processing application software
Primary Device ID08056304454065
NIH Device Record Keye0fa35cb-d3f5-484e-97bd-a13c649c133f
Commercial Distribution StatusIn Commercial Distribution
Brand NameCAAS IntraVascular
Version Model Number2.1
Company DUNS413761941
Company NamePie Medical Imaging B.V.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+31433281328
Emailsupport@pie.nl
Phone+31433281328
Emailsupport@pie.nl
Phone+31433281328
Emailsupport@pie.nl
Phone+31433281328
Emailsupport@pie.nl
Phone+31433281328
Emailsupport@pie.nl
Phone+31433281328
Emailsupport@pie.nl
Phone+31433281328
Emailsupport@pie.nl
Phone+31433281328
Emailsupport@pie.nl
Phone+31433281328
Emailsupport@pie.nl
Phone+31433281328
Emailsupport@pie.nl
Phone+31433281328
Emailsupport@pie.nl
Phone+31433281328
Emailsupport@pie.nl
Phone+31433281328
Emailsupport@pie.nl
Phone+31433281328
Emailsupport@pie.nl
Phone+31433281328
Emailsupport@pie.nl
Phone+31433281328
Emailsupport@pie.nl

Device Identifiers

Device Issuing AgencyDevice ID
GS108056304454065 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LLZSystem, Image Processing, Radiological

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-10-07
Device Publish Date2018-11-22

On-Brand Devices [CAAS IntraVascular ]

080563044511871.0
080563044540652.1
080563044534712.0

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