Endo Scope Kerrision Rotating Rongeur Shaft

GUDID 08809596474095

Hankil Tech Medical Co., Ltd.

Surgical implant/trial-implant/sizer holder, reusable
Primary Device ID08809596474095
NIH Device Record Keyaa13e53c-14d1-40e8-b588-468f676c0233
Commercial Distribution StatusIn Commercial Distribution
Brand NameEndo Scope Kerrision Rotating Rongeur Shaft
Version Model Number21-464
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 Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108809596474095 [Primary]

FDA Product Code

EMHForceps, Rongeur, Surgical

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08809596474095]

Moist Heat or Steam Sterilization


[08809596474095]

Moist Heat or Steam Sterilization


[08809596474095]

Moist Heat or Steam Sterilization


[08809596474095]

Moist Heat or Steam Sterilization


[08809596474095]

Moist Heat or Steam Sterilization


[08809596474095]

Moist Heat or Steam Sterilization


[08809596474095]

Moist Heat or Steam Sterilization


[08809596474095]

Moist Heat or Steam Sterilization


[08809596474095]

Moist Heat or Steam Sterilization


[08809596474095]

Moist Heat or Steam Sterilization


[08809596474095]

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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