Kitazato OPU Needle 382124

GUDID 14580745041504

KITAZATO CORPORATION

Soft-tissue biopsy procedure kit, non-medicated
Primary Device ID14580745041504
NIH Device Record Key1c311ee9-b133-4965-894f-7bb1a16a3cc6
Commercial Distribution StatusIn Commercial Distribution
Brand NameKitazato OPU Needle
Version Model Number382124
Catalog Number382124
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
GS104580745041507 [Primary]
GS114580745041504 [Package]
Contains: 04580745041507
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 StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-10-05
Device Publish Date2022-09-27

On-Brand Devices [Kitazato OPU Needle]

14580745041856322000
14580745041849321000
14580745041832320042
04580745041828320041
14580745041818329000
14580745041801328000
04580745041798327000
14580745041788326000
14580745041504382124
14580745041498382023
14580745041481381722
14580745041474381720

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