Primary Device ID | 07640181162826 |
NIH Device Record Key | f6360f9b-845e-4f8e-9a69-d43502725d98 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Touch CMC 1 - Bone Awl |
Version Model Number | 000-A00900 |
Company DUNS | 480138827 |
Company Name | Keri Medical SA |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07640181162826 [Primary] |
SFA | Prosthesis, Finger, Semi-Constrained, Metal/Polymer |
Steralize Prior To Use | true |
Device Is Sterile | false |
[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
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-07-28 |
Device Publish Date | 2025-07-18 |
07640181160013 - TOUCH® CMC 1 | 2025-07-28 |
07640181160020 - TOUCH® CMC 1 | 2025-07-28 |
07640181160037 - TOUCH® CMC 1 | 2025-07-28 |
07640181160044 - TOUCH® CMC 1 | 2025-07-28 |
07640181160051 - TOUCH® CMC 1 | 2025-07-28 |
07640181160068 - TOUCH® CMC 1 | 2025-07-28 |
07640181160075 - TOUCH® CMC 1 | 2025-07-28 |
07640181160082 - TOUCH® CMC 1 | 2025-07-28 |