Primary Device ID | 08056304451187 |
NIH Device Record Key | fb5a2bda-cb4e-4b4c-9812-4913b12e1966 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CAAS IntraVascular |
Version Model Number | 1.0 |
Company DUNS | 413761941 |
Company Name | Pie Medical Imaging B.V. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +31308500202 |
support@pie.nl | |
Phone | +31308500202 |
support@pie.nl | |
Phone | +31308500202 |
support@pie.nl | |
Phone | +31308500202 |
support@pie.nl | |
Phone | +31308500202 |
support@pie.nl | |
Phone | +31308500202 |
support@pie.nl | |
Phone | +31308500202 |
support@pie.nl | |
Phone | +31308500202 |
support@pie.nl | |
Phone | +31308500202 |
support@pie.nl | |
Phone | +31308500202 |
support@pie.nl | |
Phone | +31308500202 |
support@pie.nl | |
Phone | +31308500202 |
support@pie.nl | |
Phone | +31308500202 |
support@pie.nl | |
Phone | +31308500202 |
support@pie.nl | |
Phone | +31308500202 |
support@pie.nl | |
Phone | +31308500202 |
support@pie.nl |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08056304451187 [Primary] |
LLZ | System, Image Processing, Radiological |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-10-07 |
Device Publish Date | 2016-09-27 |
08056304451187 | 1.0 |
08056304454065 | 2.1 |
08056304453471 | 2.0 |