Versaport
GUDID 20884521215389
Universal Fixation Cannula
Covidien LP
Laparoscopic access cannula, single-use| Primary Device ID | 20884521215389 |
| NIH Device Record Key | e5a2d2c0-cfe2-4334-b417-f6aa21790433 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Versaport |
| Version Model Number | UNVCA11STF |
| Company DUNS | 058614483 |
| Company Name | Covidien LP |
| 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 |
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.com@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.com@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.com@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.com@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.com@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.com@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.com@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.com@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.com@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.com@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.com@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.com@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.com@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.com@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.com@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.com@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.com@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.com@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 | |
| 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
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11 Millimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10884521215382 [Primary] |
| GS1 | 20884521215389 [Package] Contains: 10884521215382 Package: CASE [6 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K130435
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 | 2020-01-09 |
| Device Publish Date | 2016-09-24 |
On-Brand Devices [Versaport]
| 10884521094437 | Fixation Cannula |
| 10884521094406 | Fixation Cannula |
| 10884521093591 | Trocar Sleeve |
| 10884521093584 | Trocar Sleeve |
| 10884521081352 | V2 Bladed RT Obturator |
| 10884521081345 | V2 Bladed RT Obturator |
| 10884521081277 | V2 Bladed Trocar with Fixation Cannula |
| 10884521081260 | V2 Bladed Trocar |
| 10884521081253 | V2 Bladed Trocar with Fixation Cannula |
| 10884521081246 | V2 Bladed Trocar |
| 10884521078529 | Reusable Cannula |
| 10884521078420 | Reusable Cannula |
| 20884521215402 | Universal Fixation Cannula |
| 20884521215396 | Universal Fixation Cannula |
| 20884521215389 | Universal Fixation Cannula |
| 20884521181356 | Bladeless Optical Fixation Cannula |
| 20884521181349 | Bladeless Optical Trocar with Fixation Cannula |
| 20884521181332 | Bladeless Optical Trocar with Fixation Cannula |
| 20884521181325 | Bladeless Optical Fixation Cannula |
| 20884521134260 | Bladeless Optical Fixation Cannula |
| 20884521134253 | Bladeless Optical Fixation Cannula |
| 20884521134246 | Bladeless Optical Trocar with Fixation Cannula |
| 20884521134239 | Bladeless Optical Trocar with Fixation Cannula |
| 20884521134222 | Bladeless Optical Trocar with Fixation Cannula |
| 20884521134215 | Bladeless Optical Trocar with Fixation Cannula |
| 20884521134277 | Bladeless Optical Fixation Cannula |
| 10884521078543 | Reusable Cannula |
| 10884521078383 | Reusable Cannula |
| 10884521094420 | Trocar Sleeve |
| 10884521078536 | Reusable Cannula |
| 10884521078475 | Reusable Cannula |
| 10884521078468 | Reusable Cannula |
| 10884521078451 | Reusable Cannula |
| 10884521078444 | Reusable Cannula |
| 10884521078437 | Reusable Cannula |
| 10884521078390 | Reusable Cannula |
| 10884521078376 | Reusable Cannula |
| 20884521181400 | Bladeless Optical Fixation Cannula |
| 20884521181394 | Bladeless Optical Trocar with Fixation Cannula |
| 20884521181387 | Bladeless Optical Trocar with Fixation Cannula |
| 20884521181370 | Bladeless Optical Trocar with Smooth Cannula |
| 20884521181363 | Bladeless Optical Trocar with Fixation Cannula |
| 10884521134553 | Reusable Cannula |
| 10884521078512 | Reusable Cannula |
| 10884521094314 | Trocar Sleeve |
| 20884521076744 | Bladeless Trocar with Fixation Cannula |
| 20884521076737 | Bladeless Trocar with Fixation Cannula |
| 20884521076720 | Bladeless Trocar with Fixation Cannula |
| 20884521073514 | Fixation Cannula |
| 20884521073507 | Fixation Cannula |
Trademark Results [Versaport]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 VERSAPORT 87836696 not registered Dead/Abandoned |
Espen Technology, Inc. 2018-03-16 |
 VERSAPORT 79408710 not registered Live/Pending |
AUTOSTORE TECHNOLOGY AS 2024-08-20 |
 VERSAPORT 77970174 4007056 Live/Registered |
RA Brands, L.L.C. 2010-03-26 |
 VERSAPORT 75867342 2764625 Dead/Cancelled |
Asyst Technologies, Inc. 1999-12-08 |
 VERSAPORT 75669803 2470281 Dead/Cancelled |
MEMORY SOLUTIONS, INC. 1999-03-29 |
 VERSAPORT 75598950 not registered Dead/Abandoned |
Equator Technologies, Inc. 1998-12-02 |
 VERSAPORT 75388382 not registered Dead/Abandoned |
Prince Corporation 1997-11-12 |
 VERSAPORT 74572581 2173249 Live/Registered |
COVIDIEN LP 1994-09-12 |
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