| Primary Device ID | 06938695525000 |
| NIH Device Record Key | fd070d79-4f5f-41f4-8d50-9bfe69eb012c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Bone Filler Device |
| Version Model Number | FG2500 |
| Catalog Number | FG2500 |
| Company DUNS | 528198569 |
| Company Name | Shanghai Kinetic Medical Co., Ltd. |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +862150720558 |
| qingmeiwei@kineticmedinc.com |
| Storage Environment Humidity | Between 0 Percent (%) Relative Humidity and 80 Percent (%) Relative Humidity |
| Storage Environment Temperature | Between 18 Degrees Celsius and 25 Degrees Celsius |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06938695525000 [Primary] |
| HRX | Arthroscope |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-02-07 |
| Device Publish Date | 2016-12-05 |
| 06938695525017 | KMC Kyphoplasty System consists of four components: Balloon Catheter Tool Kit (including Bone Fi |
| 06938695525000 | KMC Kyphoplasty System consists of four components: Balloon Catheter Tool Kit (including Bone Fi |
| 06938695537713 | Bone Filler Device, Bevel Tip, 9G (3.5mm) |
| 06938695537706 | Bone Filler Device, Lateral Open Tip, 9G (3.5mm) |
| 06938695537683 | Bone Filler Device, Flat Tip, 9G (3.5mm) |