Primary Device ID | 30840143909522 |
NIH Device Record Key | 1b202060-bea7-445f-a231-3681b584aefd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FindrWIRZ |
Version Model Number | 40-05 |
Catalog Number | FG-0037 |
Company DUNS | 006133784 |
Company Name | ATRICURE, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
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 |
Phone | 866-449-2342 |
SEhlert@atricure.com | |
Phone | 866-449-2342 |
SEhlert@atricure.com | |
Phone | 866-449-2342 |
SEhlert@atricure.com | |
Phone | 866-449-2342 |
SEhlert@atricure.com | |
Phone | 866-449-2342 |
SEhlert@atricure.com | |
Phone | 866-449-2342 |
SEhlert@atricure.com | |
Phone | 866-449-2342 |
SEhlert@atricure.com | |
Phone | 866-449-2342 |
SEhlert@atricure.com | |
Phone | 866-449-2342 |
SEhlert@atricure.com | |
Phone | 866-449-2342 |
SEhlert@atricure.com | |
Phone | 866-449-2342 |
SEhlert@atricure.com | |
Phone | 866-449-2342 |
SEhlert@atricure.com | |
Phone | 866-449-2342 |
SEhlert@atricure.com | |
Phone | 866-449-2342 |
SEhlert@atricure.com |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10840143909528 [Primary] |
GS1 | 30840143909522 [Package] Contains: 10840143909528 Package: Box [1 Units] In Commercial Distribution |
GS1 | 50840143909526 [Package] Package: Case [10 Units] In Commercial Distribution |
DQX | Wire, Guide, Catheter |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-04-14 |
Device Publish Date | 2023-04-06 |
00818354017588 | FindrWIRZ Guidewire System |
10840143901751 | FindrWIRZ Guide Wire System |
30840143909522 | FindrWIRZ Guide Wire System |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() FINDRWIRZ 77540202 3719562 Live/Registered |
SentreHEART, Inc. 2008-08-06 |