Kitazato OPU Needle with Connection Tube, Type2-v17 322002

GUDID 14580303269876

22G300mm, L Stopper

KITAZATO CORPORATION

Soft-tissue biopsy procedure kit, non-medicated
Primary Device ID14580303269876
NIH Device Record Keyf568f578-bd44-4a27-8540-589c422696bf
Commercial Distribution StatusIn Commercial Distribution
Brand NameKitazato OPU Needle with Connection Tube, Type2-v17
Version Model Number322002 Type2-v17
Catalog Number322002
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
GS104580303269879 [Primary]
GS114580303269876 [Package]
Contains: 04580303269879
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-v17]

14580303269449352304 Type2-v17
1458030326987622G300mm, L Stopper

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