| Primary Device ID | ENOU17779 |
| NIH Device Record Key | d67eb5ab-20e6-4852-9e20-55b8834a0658 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Y-Splitter |
| Version Model Number | 1777 |
| Company DUNS | 480610476 |
| Company Name | Nouvag 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 | false |
| 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 |
| Phone | +41718466600 |
| info@nouvag.com |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | ENOU17779 [Primary] |
| EGS | Handpiece, Contra- And Right-Angle Attachment, Dental |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[ENOU17779]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-04-23 |
| Device Publish Date | 2018-08-21 |
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