AtriClip® PRO•V™ LAA Exclusion System A000974
GUDID 00818354015157
AtriClip® PRO•V™ LAA Exclusion System 50
ATRICURE, INC.
Ligation clip, metallic| Primary Device ID | 00818354015157 |
| NIH Device Record Key | 4f096d64-f2d1-4ef1-b0b8-7e99ac77b27a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | AtriClip® PRO•V™ LAA Exclusion System |
| Version Model Number | PROV50 |
| Catalog Number | A000974 |
| Company DUNS | 006133784 |
| Company Name | ATRICURE, INC. |
| 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 | true |
| 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 | 866-349-2342 |
| xxx@xxx.xxx | |
| Phone | 866-349-2342 |
| xxx@xxx.xxx | |
| Phone | 866-349-2342 |
| xxx@xxx.xxx | |
| Phone | 866-349-2342 |
| xxx@xxx.xxx | |
| Phone | 866-349-2342 |
| xxx@xxx.xxx | |
| Phone | 866-349-2342 |
| xxx@xxx.xxx | |
| Phone | 866-349-2342 |
| xxx@xxx.xxx | |
| Phone | 866-349-2342 |
| xxx@xxx.xxx | |
| Phone | 866-349-2342 |
| xxx@xxx.xxx | |
| Phone | 866-349-2342 |
| xxx@xxx.xxx | |
| Phone | 866-349-2342 |
| xxx@xxx.xxx | |
| Phone | 866-349-2342 |
| xxx@xxx.xxx | |
| Phone | 866-349-2342 |
| xxx@xxx.xxx |
Device Dimensions
| Length | 50 Millimeter |
| Length | 50 Millimeter |
| Length | 50 Millimeter |
| Length | 50 Millimeter |
| Length | 50 Millimeter |
| Length | 50 Millimeter |
| Length | 50 Millimeter |
| Length | 50 Millimeter |
| Length | 50 Millimeter |
| Length | 50 Millimeter |
| Length | 50 Millimeter |
| Length | 50 Millimeter |
| Length | 50 Millimeter |
Operating and Storage Conditions
| Handling Environment Temperature | Between 20 Degrees Celsius and 0 Degrees Celsius |
| Handling Environment Temperature | Between 20 Degrees Celsius and 0 Degrees Celsius |
| Handling Environment Temperature | Between 20 Degrees Celsius and 0 Degrees Celsius |
| Handling Environment Temperature | Between 20 Degrees Celsius and 0 Degrees Celsius |
| Handling Environment Temperature | Between 20 Degrees Celsius and 0 Degrees Celsius |
| Handling Environment Temperature | Between 20 Degrees Celsius and 0 Degrees Celsius |
| Handling Environment Temperature | Between 20 Degrees Celsius and 0 Degrees Celsius |
| Handling Environment Temperature | Between 20 Degrees Celsius and 0 Degrees Celsius |
| Handling Environment Temperature | Between 20 Degrees Celsius and 0 Degrees Celsius |
| Handling Environment Temperature | Between 20 Degrees Celsius and 0 Degrees Celsius |
| Handling Environment Temperature | Between 20 Degrees Celsius and 0 Degrees Celsius |
| Handling Environment Temperature | Between 20 Degrees Celsius and 0 Degrees Celsius |
| Handling Environment Temperature | Between 20 Degrees Celsius and 0 Degrees Celsius |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00818354015157 [Primary] |
FDA Product Code
| FZP | Clip, Implantable |
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 | 2018-11-15 |
| Device Publish Date | 2016-04-25 |
On-Brand Devices [AtriClip® PRO•V™ LAA Exclusion System]
| 00818354015157 | AtriClip® PRO•V™ LAA Exclusion System 50 |
| 00818354015140 | AtriClip® PRO•V™ LAA Exclusion System 45 |
| 00818354015133 | AtriClip® PRO•V™ LAA Exclusion System 40 |
| 00818354015126 | AtriClip® PRO•V™ LAA Exclusion System 35 |
| 30840143900246 | AtriClip® PRO•V™ LAA Exclusion System 50 |
| 30840143900239 | AtriClip® PRO•V™ LAA Exclusion System 45 |
| 30840143900222 | AtriClip® PRO•V™ LAA Exclusion System 40 |
| 30840143900215 | AtriClip® PRO•V™ LAA Exclusion System 35 |
| 10840143901249 | AtriClip® PRO•V™ LAA Exclusion System 50 |
| 10840143901225 | AtriClip® PRO•V™ LAA Exclusion System 45 |
| 10840143901201 | AtriClip® PRO•V™ LAA Exclusion System 40 |
| 10840143901188 | AtriClip® PRO•V™ LAA Exclusion System 35 |
| 30840143912133 | LAA Exclusion System, PROV50 |
| 30840143912126 | LAA Exclusion System, PROV45 |
| 30840143912119 | LAA Exclusion System, PROV40 |
| 30840143912102 | LAA Exclusion System, PROV35 |
Trademark Results [AtriClip]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ATRICLIP 77367229 3573736 Live/Registered |
AtriCure, Inc. 2008-01-09 |
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