Primary Device ID | 00858254006008 |
NIH Device Record Key | 231737ba-57f0-4153-9f1e-ac10f40ff95c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Venclose System EVSRF Catheter |
Version Model Number | VC-10A2.5-6F-60 |
Company DUNS | 085838983 |
Company Name | VENCLOSE INC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 |
Length | 60 Centimeter |
Length | 60 Centimeter |
Length | 60 Centimeter |
Length | 60 Centimeter |
Length | 60 Centimeter |
Length | 60 Centimeter |
Length | 60 Centimeter |
Length | 60 Centimeter |
Length | 60 Centimeter |
Length | 60 Centimeter |
Length | 60 Centimeter |
Length | 60 Centimeter |
Length | 60 Centimeter |
Length | 60 Centimeter |
Length | 60 Centimeter |
Length | 60 Centimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00858254006008 [Primary] |
GS1 | 00858254006213 [Package] Package: Box [10 Units] In Commercial Distribution |
GS1 | 00858254006237 [Package] Package: Box [5 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 | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-11-01 |
00858254006015 | Endovenous Radiofrequency Ablation (RFA) Catheter, 100cm |
00858254006008 | Endovenous Radiofrequency Ablation (RFA) Catheter, 60cm |