Lospa Knee System Instrument

GUDID 08806373895111

Patella Cailpers

Corentec Co., Ltd

General-purpose calliper, metallic General-purpose calliper, metallic General-purpose calliper, metallic General-purpose calliper, metallic General-purpose calliper, metallic General-purpose calliper, metallic General-purpose calliper, metallic General-purpose calliper, metallic General-purpose calliper, metallic General-purpose calliper, metallic General-purpose calliper, metallic General-purpose calliper, metallic General-purpose calliper, metallic General-purpose calliper, metallic General-purpose calliper, metallic General-purpose calliper, metallic General-purpose calliper, metallic
Primary Device ID08806373895111
NIH Device Record Key8f425c96-7cc7-4ebc-9575-e19dbc0482d7
Commercial Distribution StatusIn Commercial Distribution
Brand NameLospa Knee System Instrument
Version Model NumberKA.SPM.0001
Company DUNS688739895
Company NameCorentec Co., Ltd
Device Count1
DM Exemptfalse
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

Customer Support Contacts

Phone+82269374902
Emailra@corentec.com
Phone+82269374902
Emailra@corentec.com
Phone+82269374902
Emailra@corentec.com
Phone+82269374902
Emailra@corentec.com
Phone+82269374902
Emailra@corentec.com
Phone+82269374902
Emailra@corentec.com
Phone+82269374902
Emailra@corentec.com
Phone+82269374902
Emailra@corentec.com
Phone+82269374902
Emailra@corentec.com
Phone+82269374902
Emailra@corentec.com
Phone+82269374902
Emailra@corentec.com
Phone+82269374902
Emailra@corentec.com
Phone+82269374902
Emailra@corentec.com
Phone+82269374902
Emailra@corentec.com
Phone+82269374902
Emailra@corentec.com
Phone+82269374902
Emailra@corentec.com
Phone+82269374902
Emailra@corentec.com

Device Identifiers

Device Issuing AgencyDevice ID
GS108806373895111 [Primary]

FDA Product Code

KTZCaliper

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08806373895111]

Moist Heat or Steam Sterilization


[08806373895111]

Moist Heat or Steam Sterilization


[08806373895111]

Moist Heat or Steam Sterilization


[08806373895111]

Moist Heat or Steam Sterilization


[08806373895111]

Moist Heat or Steam Sterilization


[08806373895111]

Moist Heat or Steam Sterilization


[08806373895111]

Moist Heat or Steam Sterilization


[08806373895111]

Moist Heat or Steam Sterilization


[08806373895111]

Moist Heat or Steam Sterilization


[08806373895111]

Moist Heat or Steam Sterilization


[08806373895111]

Moist Heat or Steam Sterilization


[08806373895111]

Moist Heat or Steam Sterilization


[08806373895111]

Moist Heat or Steam Sterilization


[08806373895111]

Moist Heat or Steam Sterilization


[08806373895111]

Moist Heat or Steam Sterilization


[08806373895111]

Moist Heat or Steam Sterilization


[08806373895111]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-03-25
Device Publish Date2024-03-15

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08800068900722 - BENCOX Hip System2024-06-04 Bencox Delta Option Head 40S
08800068900739 - BENCOX Hip System2024-06-04 Bencox Delta Option Head 40M
08800068900746 - BENCOX Hip System2024-06-04 Bencox Delta Option Head 40L
08800068900753 - BENCOX Hip System2024-06-04 Bencox Delta Option Head 40XL
08800068900609 - BENCOX Hip System2024-06-03 BENCOX delta option head 28S

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