Primary Device ID | 20801902221692 |
NIH Device Record Key | da709429-02f9-4c30-a6d2-dc43985c2490 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | WARRIOR |
Version Model Number | IPN930526 |
Catalog Number | 7389 |
Company DUNS | 002348191 |
Company Name | TELEFLEX INCORPORATED |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
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 | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10801902221695 [Primary] |
GS1 | 20801902221692 [Package] Contains: 10801902221695 Package: Box [5 Units] In Commercial Distribution |
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 | 2025-06-12 |
Device Publish Date | 2025-06-04 |
30841156101156 | Warrior Guidewire 200cm |
30841156101163 | Warrior Guidewire 300cm |
20841156108035 | Warrior Guidewire, 200cm |
20801902168003 | Warrior Guidewire, 300cm |
20841156111431 | Warrior Guidewire 200CM |
20801902221692 | Warrior Guidewire 300CM |