AtriClip FLEX•V A001018-4

GUDID 10840143901287

AtriClip FLEX•V device 40

ATRICURE, INC.

Ligation clip, metallic
Primary Device ID10840143901287
NIH Device Record Keye22203c6-410a-46fb-a187-e12df3105a6a
Commercial Distribution StatusIn Commercial Distribution
Brand NameAtriClip FLEX•V
Version Model NumberACHV40
Catalog NumberA001018-4
Company DUNS006133784
Company NameATRICURE, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone866-349-2342
Emailxxx@xxx.xxx

Device Dimensions

Length40 Millimeter

Operating and Storage Conditions

Handling Environment TemperatureBetween 20 Degrees Celsius and 0 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS110840143901287 [Primary]

FDA Product Code

FZPClip, Implantable

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-01-13
Device Publish Date2023-01-05

On-Brand Devices [AtriClip FLEX•V]

00818354016185AtriClip FLEX•V device 50
00818354016178AtriClip FLEX•V device 45
00818354016161AtriClip FLEX•V device 40
00818354016154AtriClip FLEX•V device 35
30840143900161AtriClip FLEX•V device 50
30840143900154AtriClip FLEX•V device 45
30840143900147AtriClip FLEX•V device 40
30840143900130AtriClip FLEX•V device 35
10840143901324AtriClip FLEX•V device 50
10840143901300AtriClip FLEX•V device 45
10840143901287AtriClip FLEX•V device 40
10840143901263AtriClip FLEX•V device 35

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.