Kitazato OPU Needle with Connection Tube, Type2-v14 320001

GUDID 14580303269845

20G350mm, L Stopper

KITAZATO CORPORATION

Soft-tissue biopsy procedure kit, non-medicated
Primary Device ID14580303269845
NIH Device Record Key03e3c2d5-ef1b-4e1a-a1a0-78d34f4de60f
Commercial Distribution StatusIn Commercial Distribution
Brand NameKitazato OPU Needle with Connection Tube, Type2-v14
Version Model Number320001 Type2-v14
Catalog Number320001
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
GS104580303269848 [Primary]
GS114580303269845 [Package]
Contains: 04580303269848
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 Number2
Public Version Date2020-01-08
Device Publish Date2019-06-01

On-Brand Devices [Kitazato OPU Needle with Connection Tube, Type2-v14]

14580303269418350354 Type2-v14
1458030326984520G350mm, L Stopper

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