Bashir™ Plus Endovascular Catheter 7Fr, 12.5cm basket, 10.0cm Infusion 7210
GUDID 00850005115038
Bashir™ Plus Endovascular Catheter 7Fr, 12.5cm basket, 10.0cm Infusion
THROMBOLEX, INC.
Peripheral vascular infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter| Primary Device ID | 00850005115038 |
| NIH Device Record Key | 6885229c-7b86-4bce-be82-490df391e82c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Bashir™ Plus Endovascular Catheter 7Fr, 12.5cm basket, 10.0cm Infusion |
| Version Model Number | 7210 |
| Catalog Number | 7210 |
| Company DUNS | 080580521 |
| Company Name | THROMBOLEX, 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | 2678983986 |
| amy@thrombolex.com | |
| Phone | 2678983986 |
| amy@thrombolex.com | |
| Phone | 2678983986 |
| amy@thrombolex.com | |
| Phone | 2678983986 |
| amy@thrombolex.com | |
| Phone | 2678983986 |
| amy@thrombolex.com | |
| Phone | 2678983986 |
| amy@thrombolex.com | |
| Phone | 2678983986 |
| amy@thrombolex.com | |
| Phone | 2678983986 |
| amy@thrombolex.com | |
| Phone | 2678983986 |
| amy@thrombolex.com | |
| Phone | 2678983986 |
| amy@thrombolex.com | |
| Phone | 2678983986 |
| amy@thrombolex.com | |
| Phone | 2678983986 |
| amy@thrombolex.com | |
| Phone | 2678983986 |
| amy@thrombolex.com | |
| Phone | 2678983986 |
| amy@thrombolex.com | |
| Phone | 2678983986 |
| amy@thrombolex.com | |
| Phone | 2678983986 |
| amy@thrombolex.com | |
| Phone | 2678983986 |
| amy@thrombolex.com | |
| Phone | 2678983986 |
| amy@thrombolex.com | |
| Phone | 2678983986 |
| amy@thrombolex.com | |
| Phone | 2678983986 |
| amy@thrombolex.com | |
| Phone | 2678983986 |
| amy@thrombolex.com | |
| Phone | 2678983986 |
| amy@thrombolex.com | |
| Phone | 2678983986 |
| amy@thrombolex.com | |
| Phone | 2678983986 |
| amy@thrombolex.com | |
| Phone | 2678983986 |
| amy@thrombolex.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850005115038 [Primary] |
| GS1 | 10850005115035 [Package] Package: Carton [16 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K193071
FDA Product Code
| KRA | Catheter, Continuous Flush |
| QEY | Mechanical Thrombolysis Catheter |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-02-25 |
| Device Publish Date | 2020-02-17 |
Devices Manufactured by THROMBOLEX, INC.
| 00850005115076 - BASHIR™ .035 Endovascular Catheter | 2023-12-19 Bashir™ .035 Endovascular Catheter 8Fr, 12.5cm basket |
| 10850005115080 - BASHIR™ S-B .035 Endovascular Catheter | 2023-12-19 Bashir™ .035 S-B Endovascular Catheter 8Fr, 10.0cm basket |
| 00850005115021 - Bashir™ S-B Endovascular Catheter 7Fr, 10.0cm basket | 2020-02-25 Bashir™ S-B Endovascular Catheter 7Fr, 10.0cm basket |
| 00850005115038 - Bashir™ Plus Endovascular Catheter 7Fr, 12.5cm basket, 10.0cm Infusion | 2020-02-25Bashir™ Plus Endovascular Catheter 7Fr, 12.5cm basket, 10.0cm Infusion |
| 00850005115038 - Bashir™ Plus Endovascular Catheter 7Fr, 12.5cm basket, 10.0cm Infusion | 2020-02-25 Bashir™ Plus Endovascular Catheter 7Fr, 12.5cm basket, 10.0cm Infusion |
| 00850005115045 - Bashir™ Plus Endovascular Catheter 7Fr, 12.5cm basket, 20.0cm Infusion | 2020-02-25 Bashir™ Plus Endovascular Catheter 7Fr, 12.5cm basket, 20.0cm Infusion |
| 00850005115052 - Bashir™ Plus Endovascular Catheter 7Fr, 12.5cm basket, 30.0cm Infusion | 2020-02-25 Bashir™ Plus Endovascular Catheter 7Fr, 12.5cm basket, 30.0cm Infusion |
| 00850005115069 - Bashir™ Plus Endovascular Catheter 7Fr, 12.5cm basket, 40.0cm Infusion | 2020-02-25 Bashir™ Plus Endovascular Catheter 7Fr, 12.5cm basket, 40.0cm Infusion |
| 00850005115007 - Bashir™ Endovascular Catheter | 2020-02-11 |
Trademark Results [Bashir]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 BASHIR 88533456 not registered Live/Pending |
Thrombolex, Inc. 2019-07-24 |
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