| Primary Device ID | 16956989913064 |
| NIH Device Record Key | f6ea54d8-1c63-4cb4-b054-e7afb8dff146 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Victan |
| Version Model Number | EC-PN190A |
| Company DUNS | 421332708 |
| Company Name | Jiangsu Haize Medical Scientific Development 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 | false |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06956989913067 [Primary] |
| GS1 | 16956989913064 [Package] Contains: 06956989913067 Package: Box [5 Units] In Commercial Distribution |
| GS1 | 26956989913061 [Package] Package: Case [6 Units] In Commercial Distribution |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-06-21 |
| Device Publish Date | 2023-06-13 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() VICTAN 75687959 2411945 Live/Registered |
PODANFOL S.A. 1999-04-22 |
![]() VICTAN 73819502 1596025 Dead/Cancelled |
SANOFI 1989-08-14 |
![]() VICTAN 73402240 1284035 Dead/Cancelled |
Sanofi 1982-11-10 |