Primary Device ID | 04042409076992 |
NIH Device Record Key | c2be7045-5552-487b-992a-e089ef604960 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | SC 7016-02 |
Catalog Number | SC 7016-02 |
Company DUNS | 328420633 |
Company Name | aap Implantate AG |
Device Count | 1 |
DM Exempt | true |
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 | true |
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 | 04042409076992 [Primary] |
HWC | Screw, fixation, bone |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04042409076992]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2024-02-19 |
Device Publish Date | 2016-08-18 |
04042409449840 - NA | 2024-10-07 Cannulated Headless Bone Screw 6.5, L 75, TL 15 short, Titanium |
04042409449864 - NA | 2024-10-07 Cannulated Headless Bone Screw 6.5, L 80, TL 20 short, Titanium |
04042409449888 - NA | 2024-10-07 Cannulated Headless Bone Screw 6.5, L 85, TL 20 short, Titanium |
04042409449901 - NA | 2024-10-07 Cannulated Headless Bone Screw 6.5, L 90, TL 20 short, Titanium |
04042409449925 - NA | 2024-10-07 Cannulated Headless Bone Screw 6.5, L 95, TL 20 short, Titanium |
04042409449949 - NA | 2024-10-07 Cannulated Headless Bone Screw 6.5, L 100, TL 20 short, Titanium |
04042409449963 - NA | 2024-10-07 Cannulated Headless Bone Screw 6.5, L 105, TL 20 short, Titanium |
04042409449987 - NA | 2024-10-07 Cannulated Headless Bone Screw 6.5, L 110, TL 20 short, Titanium |