Primary Device ID | 00859975005042 |
NIH Device Record Key | 09834aa4-b077-4af6-bb38-a1313690b202 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Trivarion |
Version Model Number | 001-15 |
Company DUNS | 790584176 |
Company Name | ACTIVATEK INC. |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00859975005042 [Primary] |
GS1 | 10859975005049 [Package] Package: Shelf Box [12 Units] In Commercial Distribution |
GS1 | 20859975005046 [Package] Contains: 10859975005049 Package: Case [20 Units] In Commercial Distribution |
EGJ | Device, Iontophoresis, Other Uses |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2014-11-26 |
00859975005073 | Buffered Iontophoretic Delivery Kit- Butterfly, 2.0cc |
00859975005066 | Buffered Iontophoretic Delivery Kit- Large, 3.5cc |
00859975005059 | Buffered Iontophoretic Delivery Kit- Medium, 2.0cc |
00859975005042 | Buffered Iontophoretic Delivery Kit- Small, 1.5cc |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TRIVARION 78918189 3304700 Live/Registered |
ActivaTek, Inc. 2006-06-27 |