| Primary Device ID | 10705034005232 |
| NIH Device Record Key | 58228a89-c6a5-40ec-bee6-44b9898f3288 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | KANEDA SR |
| Version Model Number | 3210510 |
| Catalog Number | 3210510 |
| Company DUNS | 482661753 |
| Company Name | Medos International Sàrl |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| 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 | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10705034005232 [Primary] |
| HWJ | AWL |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[10705034005232]
Moist Heat or Steam Sterilization
[10705034005232]
Moist Heat or Steam Sterilization
[10705034005232]
Moist Heat or Steam Sterilization
[10705034005232]
Moist Heat or Steam Sterilization
[10705034005232]
Moist Heat or Steam Sterilization
[10705034005232]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2022-06-10 |
| Device Publish Date | 2016-12-31 |
| 10705034005270 | KANEDA SR ANTERIOR SYSTEM PLATE HOLDER |
| 10705034005232 | KANEDA SR ANTERIOR SYSTEM ANGLED AWL (MODULAR) |
| 10705034005225 | KANEDA SR ANTERIOR SYSTEM AWL (MODULAR) |