Primary Device ID | 04042409201905 |
NIH Device Record Key | bccf451c-25ef-44f7-a344-113ea01a6259 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | SC 6532-03-2 |
Catalog Number | SC 6532-03-2 |
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 | 04042409201905 [Primary] |
HWC | Screw, fixation, bone |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04042409201905]
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 |
04042409107320 - NA | 2024-06-14 Elevatorium bended, width 6mm, blunt |
04042409220210 - NA | 2024-06-14 Raspatory, long curved |
04042409261053 - NA | 2024-06-14 Elevatorium bended, width 3mm, sharp |
04042409359835 - NA | 2024-06-14 Elevatorium bended, width 6mm, sharp |
04042409047657 - NA | 2024-02-19 K-wire with trocar point, ø0.8, L 150 |
04042409047695 - NA | 2024-02-19 K-wire with trocar point, ø0.8, L 310 |
04042409047701 - NA | 2024-02-19 K-wire with trocar point, ø1.0, L 100 |
04042409047718 - NA | 2024-02-19 K-wire with trocar point, ø1.0, L 150 |