| Primary Device ID | 07290110483012 |
| NIH Device Record Key | c609d6f7-fc75-4568-ada9-8e1b00871bf9 |
| Commercial Distribution Discontinuation | 2017-09-30 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | NESS L300-Plus System |
| Version Model Number | L3P-5000 |
| Catalog Number | 501-00123-01 |
| Company DUNS | 182287727 |
| Company Name | BIONESS INC. |
| 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 | true |
| 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 | +97297907100 |
| info@bioness.co.il | |
| Phone | +97297907100 |
| info@bioness.co.il | |
| Phone | +97297907100 |
| info@bioness.co.il | |
| Phone | +97297907100 |
| info@bioness.co.il | |
| Phone | +97297907100 |
| info@bioness.co.il | |
| Phone | +97297907100 |
| info@bioness.co.il | |
| Phone | +97297907100 |
| info@bioness.co.il | |
| Phone | +97297907100 |
| info@bioness.co.il | |
| Phone | +97297907100 |
| info@bioness.co.il | |
| Phone | +97297907100 |
| info@bioness.co.il |
| Storage Environment Temperature | Between -25 Degrees Celsius and 55 Degrees Celsius |
| Storage Environment Temperature | Between -25 Degrees Celsius and 55 Degrees Celsius |
| Special Storage Condition, Specify | Between 0 and 0 *Degrees Celsius |
| Storage Environment Temperature | Between -25 Degrees Celsius and 55 Degrees Celsius |
| Special Storage Condition, Specify | Between 0 and 0 *Degrees Celsius |
| Storage Environment Temperature | Between -25 Degrees Celsius and 55 Degrees Celsius |
| Special Storage Condition, Specify | Between 0 and 0 *Degrees Celsius |
| Storage Environment Temperature | Between -25 Degrees Celsius and 55 Degrees Celsius |
| Special Storage Condition, Specify | Between 0 and 0 *Degrees Celsius |
| Storage Environment Temperature | Between -25 Degrees Celsius and 55 Degrees Celsius |
| Special Storage Condition, Specify | Between 0 and 0 *Degrees Celsius |
| Storage Environment Temperature | Between -25 Degrees Celsius and 55 Degrees Celsius |
| Special Storage Condition, Specify | Between 0 and 0 *Degrees Celsius |
| Storage Environment Temperature | Between -25 Degrees Celsius and 55 Degrees Celsius |
| Special Storage Condition, Specify | Between 0 and 0 *Degrees Celsius |
| Storage Environment Temperature | Between -25 Degrees Celsius and 55 Degrees Celsius |
| Special Storage Condition, Specify | Between 0 and 0 *Degrees Celsius |
| Storage Environment Temperature | Between -25 Degrees Celsius and 55 Degrees Celsius |
| Special Storage Condition, Specify | Between 0 and 0 *Degrees Celsius |
| Storage Environment Temperature | Between -25 Degrees Celsius and 55 Degrees Celsius |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07290110483012 [Primary] |
| IPF | Stimulator, muscle, powered |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-11-08 |
| Device Publish Date | 2017-02-02 |
| 07290110483043 | L300 Plus US Clinician's Upgrade Kit |
| 07290110483036 | L300 Plus US Upgrade System Kit, Right (regular) |
| 07290110483029 | L300 Plus US Upgrade System Kit, Left (regular) |
| 07290110483012 | L300 Plus US System Kit, Right (regular) |
| 07290110483005 | L300 Plus US System Kit, Left (regular) |