Primary Device ID | 08056304453044 |
NIH Device Record Key | 0b326445-016e-416b-9f18-f5d1a0b9e2c8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CAAS MRV |
Version Model Number | 4.2 |
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 | 08056304453044 [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 | 2017-01-18 |
08056304451163 | 3.0 |
08056304453426 | 4.3 |
08056304453044 | 4.2 |