Kitazato OPU Needle Type2-v6 351304

GUDID 14580303269142

KITAZATO CORPORATION

Soft-tissue biopsy procedure kit, non-medicated
Primary Device ID14580303269142
NIH Device Record Key920c1405-e032-48a8-bc9d-a63a8b289a17
Commercial Distribution StatusIn Commercial Distribution
Brand NameKitazato OPU Needle Type2-v6
Version Model Number351304 Type2-v6
Catalog Number351304
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
GS104580303269145 [Primary]
GS114580303269142 [Package]
Contains: 04580303269145
Package: [10 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MQENEEDLE, ASSISTED REPRODUCTION

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-01-08
Device Publish Date2016-11-09

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