ProTack
GUDID 20884521070407
Fixation Device
Covidien LP
Soft-tissue/mesh anchor, non-bioabsorbable| Primary Device ID | 20884521070407 |
| NIH Device Record Key | 8e723475-ac10-4a4a-82b5-3a282d3df005 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ProTack |
| Version Model Number | 174006 |
| Company DUNS | 058614483 |
| Company Name | Covidien LP |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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 |
Customer Support Contacts
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com |
Device Dimensions
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
Operating and Storage Conditions
| Handling Environment Temperature | Between 0 Degrees Fahrenheit and 130 Degrees Fahrenheit |
| Handling Environment Temperature | Between 0 Degrees Fahrenheit and 130 Degrees Fahrenheit |
| Handling Environment Temperature | Between 0 Degrees Fahrenheit and 130 Degrees Fahrenheit |
| Handling Environment Temperature | Between 0 Degrees Fahrenheit and 130 Degrees Fahrenheit |
| Handling Environment Temperature | Between 0 Degrees Fahrenheit and 130 Degrees Fahrenheit |
| Handling Environment Temperature | Between 0 Degrees Fahrenheit and 130 Degrees Fahrenheit |
| Handling Environment Temperature | Between 0 Degrees Fahrenheit and 130 Degrees Fahrenheit |
| Handling Environment Temperature | Between 0 Degrees Fahrenheit and 130 Degrees Fahrenheit |
| Handling Environment Temperature | Between 0 Degrees Fahrenheit and 130 Degrees Fahrenheit |
| Handling Environment Temperature | Between 0 Degrees Fahrenheit and 130 Degrees Fahrenheit |
| Handling Environment Temperature | Between 0 Degrees Fahrenheit and 130 Degrees Fahrenheit |
| Handling Environment Temperature | Between 0 Degrees Fahrenheit and 130 Degrees Fahrenheit |
| Handling Environment Temperature | Between 0 Degrees Fahrenheit and 130 Degrees Fahrenheit |
| Handling Environment Temperature | Between 0 Degrees Fahrenheit and 130 Degrees Fahrenheit |
| Handling Environment Temperature | Between 0 Degrees Fahrenheit and 130 Degrees Fahrenheit |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10884521070400 [Primary] |
| GS1 | 20884521070407 [Package] Contains: 10884521070400 Package: CASE [6 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K090470
FDA Product Code
| GCJ | Laparoscope, general & plastic surgery |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2024-05-16 |
| Device Publish Date | 2016-09-24 |
Devices Manufactured by Covidien LP
| 20884521826264 - MaxTack | 2024-09-17 Motorized Fixation Device 30 Absorbable Tacks |
| 10884521844704 - Microstream | 2024-09-16 Microstream CO2 NanoPod |
| 10884521849358 - Vital Sync | 2024-09-09 VITAL SYNC V4 SOFTWARE |
| 20884521066493 - Fred | 2024-08-30 Anti-Fog Kit |
| 10884521837102 - ILLUMISITE | 2024-08-19 Console |
| 10884521837126 - ILLUMISITE | 2024-08-19 Console |
| 10884521837133 - ILLUMISITE | 2024-08-19 Console |
| 10884521837140 - ILLUMISITE | 2024-08-19 Console |
Trademark Results [ProTack]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PROTACK 76518882 2822943 Live/Registered |
WEAVER LEATHER, LLC 2003-05-08 |
 PROTACK 76518473 2859674 Dead/Cancelled |
WEAVER LEATHER, LLC 2003-05-08 |
 PROTACK 76201525 not registered Dead/Abandoned |
PROLIFIX LIMITED 2001-01-29 |
 PROTACK 76190082 2568436 Dead/Cancelled |
BOMAG AMERICAS, INC. 2001-01-08 |
 PROTACK 75228973 2251726 Live/Registered |
COVIDIEN LP 1997-01-21 |
 PROTACK 73761034 1585293 Dead/Cancelled |
ENKA B.V. 1988-10-31 |
 PROTACK 73582882 1409437 Live/Registered |
COASTAL PET PRODUCTS, INC. 1986-02-14 |
 PROTACK 73412344 1277194 Dead/Cancelled |
Prosol Corporation 1983-02-04 |
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