Kitazato IUI Catheter without Stainless Steel Center Core Type2-v1 100103

GUDID 14580303269067

KITAZATO CORPORATION

Assisted reproduction transfer catheter/set
Primary Device ID14580303269067
NIH Device Record Key755cae36-9307-487f-a3e0-101eca671943
Commercial Distribution StatusIn Commercial Distribution
Brand NameKitazato IUI Catheter without Stainless Steel Center Core Type2-v1
Version Model Number100103 Type2-v1
Catalog Number100103
Company DUNS711091157
Company NameKITAZATO CORPORATION
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 Numbertrue
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS104580303269060 [Primary]
GS114580303269067 [Package]
Contains: 04580303269060
Package: [10 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MQFCATHETER, ASSISTED REPRODUCTION

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-01-09
Device Publish Date2016-11-09

Devices Manufactured by KITAZATO CORPORATION

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14573316385534 - VS(Vitrification Solution) Pack 4 vials 4ml2024-10-25 VS(Vitrification Solution) Pack of 4x4ml vials
14573316385558 - DS(Diluent Solution) Pack 4 vials2024-10-25 DS(Diluent Solution) Pack of 4x4ml vials

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