Primary Device ID | 04042409048579 |
NIH Device Record Key | 92ce6381-cb2f-4d00-85f3-127faf8a88c7 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | NK 0127-23 |
Company DUNS | 328420633 |
Company Name | aap Implantate AG |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | 04042409048579 [Primary] |
GFC | DRIVER, SURGICAL, PIN |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04042409048579]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2024-02-19 |
Device Publish Date | 2018-02-28 |
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 |
04042409047725 - NA | 2024-02-19 K-wire with trocar point, ø1.0, L 150 |
04042409047732 - NA | 2024-02-19 K-wire with trocar point, ø1.0, L 200 |
04042409047749 - NA | 2024-02-19 K-wire with trocar point, ø1.0, L 250 |
04042409047763 - NA | 2024-02-19 K-wire with trocar point, ø1.0, L 310 |