| Primary Device ID | 06924274954231 |
| NIH Device Record Key | 71ddd714-44f5-40e7-8e7e-9d2d6317add7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Disposable Electrode Serie |
| Version Model Number | OB-2012 |
| Company DUNS | 421340711 |
| Company Name | Zhejiang Shuyou Surgical Instrument 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06924274954200 [Primary] |
| GS1 | 06924274954217 [Package] Contains: 06924274954200 Package: [5 Units] In Commercial Distribution |
| GS1 | 06924274954224 [Package] Contains: 06924274954217 Package: [10 Units] In Commercial Distribution |
| GS1 | 06924274954231 [Package] Contains: 06924274954224 Package: [10 Units] In Commercial Distribution |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories |
| 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 | 2016-11-14 |