Primary Device ID | 08809946780401 |
NIH Device Record Key | 0a792629-fa18-46a5-ab47-0c610897df21 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HKT Anatomical Locking Trauma System |
Version Model Number | 16203-04030 |
Catalog Number | 16203-04030 |
Company DUNS | 688499031 |
Company Name | Hankil Tech Medical Co., Ltd. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +821090544233 |
yh_park@ostymeditech.com | |
Phone | +821090544233 |
yh_park@ostymeditech.com | |
Phone | +821090544233 |
yh_park@ostymeditech.com | |
Phone | +821090544233 |
yh_park@ostymeditech.com | |
Phone | +821090544233 |
yh_park@ostymeditech.com | |
Phone | +821090544233 |
yh_park@ostymeditech.com | |
Phone | +821090544233 |
yh_park@ostymeditech.com | |
Phone | +821090544233 |
yh_park@ostymeditech.com | |
Phone | +821090544233 |
yh_park@ostymeditech.com | |
Phone | +821090544233 |
yh_park@ostymeditech.com | |
Phone | +821090544233 |
yh_park@ostymeditech.com | |
Phone | +821090544233 |
yh_park@ostymeditech.com | |
Phone | +821090544233 |
yh_park@ostymeditech.com | |
Phone | +821090544233 |
yh_park@ostymeditech.com | |
Phone | +821090544233 |
yh_park@ostymeditech.com | |
Phone | +821090544233 |
yh_park@ostymeditech.com | |
Phone | +821090544233 |
yh_park@ostymeditech.com |
Outer Diameter | 3 Millimeter |
Outer Diameter | 3 Millimeter |
Outer Diameter | 3 Millimeter |
Outer Diameter | 3 Millimeter |
Outer Diameter | 3 Millimeter |
Outer Diameter | 3 Millimeter |
Outer Diameter | 3 Millimeter |
Outer Diameter | 3 Millimeter |
Outer Diameter | 3 Millimeter |
Outer Diameter | 3 Millimeter |
Outer Diameter | 3 Millimeter |
Outer Diameter | 3 Millimeter |
Outer Diameter | 3 Millimeter |
Outer Diameter | 3 Millimeter |
Outer Diameter | 3 Millimeter |
Outer Diameter | 3 Millimeter |
Outer Diameter | 3 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08809946780401 [Primary] |
FZX | Guide, Surgical, Instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[08809946780401]
Moist Heat or Steam Sterilization
[08809946780401]
Moist Heat or Steam Sterilization
[08809946780401]
Moist Heat or Steam Sterilization
[08809946780401]
Moist Heat or Steam Sterilization
[08809946780401]
Moist Heat or Steam Sterilization
[08809946780401]
Moist Heat or Steam Sterilization
[08809946780401]
Moist Heat or Steam Sterilization
[08809946780401]
Moist Heat or Steam Sterilization
[08809946780401]
Moist Heat or Steam Sterilization
[08809946780401]
Moist Heat or Steam Sterilization
[08809946780401]
Moist Heat or Steam Sterilization
[08809946780401]
Moist Heat or Steam Sterilization
[08809946780401]
Moist Heat or Steam Sterilization
[08809946780401]
Moist Heat or Steam Sterilization
[08809946780401]
Moist Heat or Steam Sterilization
[08809946780401]
Moist Heat or Steam Sterilization
[08809946780401]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-08-21 |
Device Publish Date | 2024-08-13 |
08809407600583 | 11424-92015 |
08809946780449 | Hex Driver Shaft Tip, 2.5 |
08809946780425 | 3.0x140mm/Dual Flat Shank drill bit |
08809946780401 | 3.0mm Variable Drill Guide (w/ Grip) |
08809596471872 | 12203-35028 |
08809596471858 | 12203-35024 |