Primary Device ID | 28717648079584 |
NIH Device Record Key | a4a089c7-2409-454a-a5d3-7f738d040742 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HI-TORQUE EXTRA S'PORT |
Version Model Number | 22225M-175 |
Catalog Number | 22225M-175 |
Company DUNS | 964569052 |
Company Name | ABBOTT VASCULAR INC. |
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 | 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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)227-9902 |
AV.CUSTOMERCARE@AV.ABBOTT.COM | |
Phone | +1(800)227-9902 |
AV.CUSTOMERCARE@AV.ABBOTT.COM | |
Phone | +1(800)227-9902 |
AV.CUSTOMERCARE@AV.ABBOTT.COM | |
Phone | +1(800)227-9902 |
AV.CUSTOMERCARE@AV.ABBOTT.COM | |
Phone | +1(800)227-9902 |
AV.CUSTOMERCARE@AV.ABBOTT.COM | |
Phone | +1(800)227-9902 |
AV.CUSTOMERCARE@AV.ABBOTT.COM | |
Phone | +1(800)227-9902 |
AV.CUSTOMERCARE@AV.ABBOTT.COM | |
Phone | +1(800)227-9902 |
AV.CUSTOMERCARE@AV.ABBOTT.COM | |
Phone | +1(800)227-9902 |
AV.CUSTOMERCARE@AV.ABBOTT.COM | |
Phone | +1(800)227-9902 |
AV.CUSTOMERCARE@AV.ABBOTT.COM | |
Phone | +1(800)227-9902 |
AV.CUSTOMERCARE@AV.ABBOTT.COM | |
Phone | +1(800)227-9902 |
AV.CUSTOMERCARE@AV.ABBOTT.COM | |
Phone | +1(800)227-9902 |
AV.CUSTOMERCARE@AV.ABBOTT.COM | |
Phone | +1(800)227-9902 |
AV.CUSTOMERCARE@AV.ABBOTT.COM | |
Phone | +1(800)227-9902 |
AV.CUSTOMERCARE@AV.ABBOTT.COM | |
Phone | +1(800)227-9902 |
AV.CUSTOMERCARE@AV.ABBOTT.COM | |
Phone | +1(800)227-9902 |
AV.CUSTOMERCARE@AV.ABBOTT.COM | |
Phone | +1(800)227-9902 |
AV.CUSTOMERCARE@AV.ABBOTT.COM |
Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08717648079580 [Primary] |
GS1 | 28717648079584 [Package] Contains: 08717648079580 Package: Case [5 Units] In Commercial Distribution |
DQX | WIRE, GUIDE, CATHETER |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2020-03-23 |
Device Publish Date | 2016-02-19 |