Primary Device ID | 10840143901287 |
NIH Device Record Key | e22203c6-410a-46fb-a187-e12df3105a6a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AtriClip FLEX•V |
Version Model Number | ACHV40 |
Catalog Number | A001018-4 |
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 | false |
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 |
Phone | 866-349-2342 |
xxx@xxx.xxx |
Length | 40 Millimeter |
Handling Environment Temperature | Between 20 Degrees Celsius and 0 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10840143901287 [Primary] |
FZP | Clip, Implantable |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-01-13 |
Device Publish Date | 2023-01-05 |
00818354016185 | AtriClip FLEX•V device 50 |
00818354016178 | AtriClip FLEX•V device 45 |
00818354016161 | AtriClip FLEX•V device 40 |
00818354016154 | AtriClip FLEX•V device 35 |
30840143900161 | AtriClip FLEX•V device 50 |
30840143900154 | AtriClip FLEX•V device 45 |
30840143900147 | AtriClip FLEX•V device 40 |
30840143900130 | AtriClip FLEX•V device 35 |
10840143901324 | AtriClip FLEX•V device 50 |
10840143901300 | AtriClip FLEX•V device 45 |
10840143901287 | AtriClip FLEX•V device 40 |
10840143901263 | AtriClip FLEX•V device 35 |