Primary Device ID | 00818075010011 |
NIH Device Record Key | 66975e68-9c26-44d2-85b8-dde93d943270 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Aristotle |
Version Model Number | 14-200-002 |
Catalog Number | A14-200-002 |
Company DUNS | 011234178 |
Company Name | SCIENTIA VASCULAR LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 888-385-9016 |
info@scientiavascular.com |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry, keep away from heat |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00818075010011 [Primary] |
DQX | Wire, Guide, Catheter |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-03-03 |
Device Publish Date | 2020-02-24 |
00818075010110 | Guidewire-Support |
00818075010103 | Guidewire-Standard |
00818075010097 | Guidewire-Soft |
00818075010035 | Guidewire- Support |
00818075010028 | Guidewire - Soft |
00818075010011 | Guidewire- Support |
00818075010004 | Guidewire-Soft |
00818075010141 | Guidewire-Support |
00818075010134 | Guidewire-Standard |
00818075010127 | Guidewire-Soft |
00818075010691 | Guidewire - Standard |
00818075011018 | Guidewire - Standard |
00818075010264 | Guidewire 300cm Extra Support |
00818075010257 | Guidewire 300cm Support |
00818075010240 | Guidewire 200cm Extra Support |
00818075010233 | Guidewire 200cm Support |