| Primary Device ID | 08052049500210 |
| NIH Device Record Key | 7d4e38dd-b1c3-40de-971d-d4a4fcec434e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NUERA TIGHT 1ch Paris Edition |
| Version Model Number | APMD145-1ch.US-PH |
| Company DUNS | 443571203 |
| Company Name | BIOS SRL |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08052049500210 [Primary] |
| PBX | Massager, Vacuum, Radio Frequency Induced Heat |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-07-14 |
| Device Publish Date | 2022-07-06 |
| 08052049500234 - Splendor X | 2024-07-10 |
| 08052049500241 - Splendor X | 2024-07-10 |
| 08052049500258 - Splendor X | 2024-07-10 |
| 08052049500265 - Splendor X | 2024-07-10 |
| 08052049500289 - OptiPLUS | 2023-11-14 |
| 08052049500272 - OptiPLUS | 2023-08-31 |
| 08052049500227 - OptiStream | 2022-10-12 |
| 08052049500210 - NUERA TIGHT 1ch Paris Edition | 2022-07-14 |
| 08052049500210 - NUERA TIGHT 1ch Paris Edition | 2022-07-14 |