CROWNJUN Double Retractor 0KEQ12WTGF

GUDID 04946585234620

KONO SEISAKUSHO CO.,LTD.

Soft-tissue surgical hook, single-use Soft-tissue surgical hook, single-use Soft-tissue surgical hook, single-use Soft-tissue surgical hook, single-use Soft-tissue surgical hook, single-use Soft-tissue surgical hook, single-use Soft-tissue surgical hook, single-use Soft-tissue surgical hook, single-use Soft-tissue surgical hook, single-use Soft-tissue surgical hook, single-use Soft-tissue surgical hook, single-use Soft-tissue surgical hook, single-use Soft-tissue surgical hook, single-use Soft-tissue surgical hook, single-use Soft-tissue surgical hook, single-use Soft-tissue surgical hook, single-use Soft-tissue surgical hook, single-use
Primary Device ID04946585234620
NIH Device Record Key7bd99230-dba0-4153-8806-b50413790827
Commercial Distribution StatusIn Commercial Distribution
Brand NameCROWNJUN Double Retractor
Version Model Number0KEQ12WTGF
Catalog Number0KEQ12WTGF
Company DUNS691486468
Company NameKONO SEISAKUSHO CO.,LTD.
Device Count1
DM Exempttrue
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
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
GS104946585234620 [Primary]
GS114946585234627 [Package]
Package: [50 Units]
In Commercial Distribution

FDA Product Code

GADRetractor

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-03-27
Device Publish Date2023-03-17

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