VENA TECH™ 4439985

GUDID 04027478130318

VENATECH® LP-BRACHIAL INTRODUCER SYSTEM

B BRAUN INTERVENTIONAL SYSTEMS, INC

Vena cava filter, permanent
Primary Device ID04027478130318
NIH Device Record Key1fab3fa4-f111-49d7-9ee1-17203db1f3ae
Commercial Distribution StatusIn Commercial Distribution
Brand NameVENA TECH™
Version Model Number4439985
Catalog Number4439985
Company DUNS784259751
Company NameB BRAUN INTERVENTIONAL SYSTEMS, INC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
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 Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(877)836-2228
Email[email protected]

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *STORE AT ROOM TEMPERATURE.

Device Identifiers

Device Issuing AgencyDevice ID
GS104027478130318 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DTKFILTER, INTRAVASCULAR, CARDIOVASCULAR

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-03-25
Device Publish Date2016-08-09

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04046964314698 - Z-MED X™2020-03-25 Z-MED-X 18X3X10X8X100X.035 PDZ432
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