Avigo™ Hydrophilic Guidewire
GUDID 00763000338275
GUIDEWIRE 103-0606-200 V04 AVIGO
Micro Therapeutics, Inc.
Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual| Primary Device ID | 00763000338275 |
| NIH Device Record Key | 9fbe963e-468f-479e-954f-8d1c308da233 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Avigo™ Hydrophilic Guidewire |
| Version Model Number | 103-0606-200 |
| Company DUNS | 826110710 |
| Company Name | Micro Therapeutics, 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
Operating and Storage Conditions
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 90 Degrees Fahrenheit |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00763000338275 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K113454
FDA Product Code
| DQX | Wire, guide, catheter |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2021-12-22 |
| Device Publish Date | 2021-05-01 |
Devices Manufactured by Micro Therapeutics, Inc.
| 00847536036215 - PipelineTM Vantage Embolization Device with Shield TechnologyTM | 2024-01-08 STENT PED3-021-250-10 V03 VANTAGE |
| 00847536036222 - PipelineTM Vantage Embolization Device with Shield TechnologyTM | 2024-01-08 STENT PED3-021-250-12 V03 VANTAGE |
| 00847536036239 - PipelineTM Vantage Embolization Device with Shield TechnologyTM | 2024-01-08 STENT PED3-021-250-14 V03 VANTAGE |
| 00847536036246 - PipelineTM Vantage Embolization Device with Shield TechnologyTM | 2024-01-08 STENT PED3-021-250-16 V03 VANTAGE |
| 00847536036253 - PipelineTM Vantage Embolization Device with Shield TechnologyTM | 2024-01-08 STENT PED3-021-250-18 V03 VANTAGE |
| 00847536036260 - PipelineTM Vantage Embolization Device with Shield TechnologyTM | 2024-01-08 STENT PED3-021-250-20 V03 VANTAGE |
| 00847536036277 - PipelineTM Vantage Embolization Device with Shield TechnologyTM | 2024-01-08 STENT PED3-021-275-10 V03 VANTAGE |
| 00847536036284 - PipelineTM Vantage Embolization Device with Shield TechnologyTM | 2024-01-08 STENT PED3-021-275-12 V03 VANTAGE |
Trademark Results [Avigo]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 AVIGO 98323474 not registered Live/Pending |
DACHSER SE 2023-12-20 |
 AVIGO 86225538 not registered Dead/Abandoned |
Reynolds Innovations Inc. 2014-03-19 |
 AVIGO 85646670 4329450 Live/Registered |
COVIDIEN LP 2012-06-08 |
 AVIGO 79231310 not registered Live/Pending |
Avigo GmbH 2017-11-16 |
 AVIGO 79209733 5466691 Live/Registered |
Avigo GmbH 2017-03-16 |
 AVIGO 77979995 3843144 Live/Registered |
TRU KIDS INC. 2008-04-28 |
 AVIGO 77466496 4084197 Live/Registered |
TRU KIDS INC. 2008-05-06 |
 AVIGO 77465660 not registered Dead/Abandoned |
GEOFFREY, LLC 2008-05-05 |
 AVIGO 77459631 not registered Dead/Abandoned |
GEOFFREY, LLC 2008-04-28 |
 AVIGO 75317407 not registered Dead/Abandoned |
TEXAS INSTRUMENTS INCORPORATED 1997-06-30 |
 AVIGO 75008364 not registered Dead/Abandoned |
Ameritech Corporation 1995-10-23 |
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