| Primary Device ID | ENOU5053MNOU0 |
| NIH Device Record Key | 0cb27897-cf9b-43f5-8fd0-9e2e5393e24a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Contra Angle 20:1 Mini |
| Version Model Number | 5053mnou |
| Company DUNS | 480610476 |
| Company Name | Nouvag 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 | false |
| Serial Number | true |
| 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 |
| Phone | +41718466600 |
| info@nouvag.com |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | ENOU5053MNOU0 [Primary] |
| EGS | Handpiece, Contra- And Right-Angle Attachment, Dental |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[ENOU5053MNOU0]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-08-09 |
| Device Publish Date | 2019-05-21 |
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