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 |