Endo Scope Kerrision Rotating Rongeur Shaft

GUDID 08809596474071

Hankil Tech Medical Co., Ltd.

Surgical implant/trial-implant/sizer holder, reusable
Primary Device ID08809596474071
NIH Device Record Key95131562-0732-4547-82d2-15f4e1ce7ec3
Commercial Distribution StatusIn Commercial Distribution
Brand NameEndo Scope Kerrision Rotating Rongeur Shaft
Version Model Number21-462
Company DUNS688499031
Company NameHankil Tech Medical 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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numbertrue
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108809596474071 [Primary]

FDA Product Code

EMHForceps, Rongeur, Surgical

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08809596474071]

Moist Heat or Steam Sterilization


[08809596474071]

Moist Heat or Steam Sterilization


[08809596474071]

Moist Heat or Steam Sterilization


[08809596474071]

Moist Heat or Steam Sterilization


[08809596474071]

Moist Heat or Steam Sterilization


[08809596474071]

Moist Heat or Steam Sterilization


[08809596474071]

Moist Heat or Steam Sterilization


[08809596474071]

Moist Heat or Steam Sterilization


[08809596474071]

Moist Heat or Steam Sterilization


[08809596474071]

Moist Heat or Steam Sterilization


[08809596474071]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-12-24
Device Publish Date2025-12-16

On-Brand Devices [Endo Scope Kerrision Rotating Rongeur Shaft]

0880959647409521-464
0880959647407121-462

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