Touch CMC 1 - Bone Awl

GUDID 07640181162826

Keri Medical SA

Orthopaedic surgical procedure kit, non-medicated, reusable
Primary Device ID07640181162826
NIH Device Record Keyf6360f9b-845e-4f8e-9a69-d43502725d98
Commercial Distribution StatusIn Commercial Distribution
Brand NameTouch CMC 1 - Bone Awl
Version Model Number000-A00900
Company DUNS480138827
Company NameKeri Medical SA
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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
GS107640181162826 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

SFAProsthesis, Finger, Semi-Constrained, Metal/Polymer

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07640181162826]

Moist Heat or Steam Sterilization


[07640181162826]

Moist Heat or Steam Sterilization


[07640181162826]

Moist Heat or Steam Sterilization


[07640181162826]

Moist Heat or Steam Sterilization


[07640181162826]

Moist Heat or Steam Sterilization


[07640181162826]

Moist Heat or Steam Sterilization


[07640181162826]

Moist Heat or Steam Sterilization


[07640181162826]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-07-28
Device Publish Date2025-07-18

Devices Manufactured by Keri Medical SA

07640181160013 - TOUCH® CMC 12025-07-28
07640181160020 - TOUCH® CMC 12025-07-28
07640181160037 - TOUCH® CMC 12025-07-28
07640181160044 - TOUCH® CMC 12025-07-28
07640181160051 - TOUCH® CMC 12025-07-28
07640181160068 - TOUCH® CMC 12025-07-28
07640181160075 - TOUCH® CMC 12025-07-28
07640181160082 - TOUCH® CMC 12025-07-28

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