| Primary Device ID | 07640172552919 |
| NIH Device Record Key | df6b7996-5e18-478e-89a1-cf0d001c3a40 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VADER Pedicle System, K-wire, Nitinol, Ø 1.1 x 600 mm |
| Version Model Number | 42-542-1 |
| Catalog Number | 42-542-1 |
| Company DUNS | 480789465 |
| Company Name | icotec AG |
| 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 | false |
| 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 |
| Phone | +417570000 |
| info@icotec.ch | |
| Phone | +417570000 |
| info@icotec.ch | |
| Phone | +417570000 |
| info@icotec.ch | |
| Phone | +417570000 |
| info@icotec.ch | |
| Phone | +417570000 |
| info@icotec.ch | |
| Phone | +417570000 |
| info@icotec.ch | |
| Phone | +417570000 |
| info@icotec.ch | |
| Phone | +417570000 |
| info@icotec.ch | |
| Phone | +417570000 |
| info@icotec.ch | |
| Phone | +417570000 |
| info@icotec.ch | |
| Phone | +417570000 |
| info@icotec.ch | |
| Phone | +417570000 |
| info@icotec.ch | |
| Phone | +417570000 |
| info@icotec.ch | |
| Phone | +417570000 |
| info@icotec.ch | |
| Phone | +417570000 |
| info@icotec.ch | |
| Phone | +417570000 |
| info@icotec.ch | |
| Phone | +417570000 |
| info@icotec.ch | |
| Phone | +417570000 |
| info@icotec.ch | |
| Phone | +417570000 |
| info@icotec.ch | |
| Phone | +417570000 |
| info@icotec.ch | |
| Phone | +417570000 |
| info@icotec.ch | |
| Phone | +417570000 |
| info@icotec.ch | |
| Phone | +417570000 |
| info@icotec.ch |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07640172552919 [Primary] |
| PML | Bone Cement, Posterior Screw Augmentation |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07640172552919]
Moist Heat or Steam Sterilization
[07640172552919]
Moist Heat or Steam Sterilization
[07640172552919]
Moist Heat or Steam Sterilization
[07640172552919]
Moist Heat or Steam Sterilization
[07640172552919]
Moist Heat or Steam Sterilization
[07640172552919]
Moist Heat or Steam Sterilization
[07640172552919]
Moist Heat or Steam Sterilization
[07640172552919]
Moist Heat or Steam Sterilization
[07640172552919]
Moist Heat or Steam Sterilization
[07640172552919]
Moist Heat or Steam Sterilization
[07640172552919]
Moist Heat or Steam Sterilization
[07640172552919]
Moist Heat or Steam Sterilization
[07640172552919]
Moist Heat or Steam Sterilization
[07640172552919]
Moist Heat or Steam Sterilization
[07640172552919]
Moist Heat or Steam Sterilization
[07640172552919]
Moist Heat or Steam Sterilization
[07640172552919]
Moist Heat or Steam Sterilization
[07640172552919]
Moist Heat or Steam Sterilization
[07640172552919]
Moist Heat or Steam Sterilization
[07640172552919]
Moist Heat or Steam Sterilization
[07640172552919]
Moist Heat or Steam Sterilization
[07640172552919]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-12-02 |
| Device Publish Date | 2024-11-22 |
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