Primary Device ID | 10858058005082 |
NIH Device Record Key | 5e74d58f-4e9d-4444-a67f-91547f98b263 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Revitive Medic |
Version Model Number | 2469MD |
Catalog Number | 2616 |
Company DUNS | 735575941 |
Company Name | ACTEGY LIMITED |
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 | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Phone | 8772603114 |
us.info@actegy.com |
Handling Environment Temperature | Between 50 Degrees Fahrenheit and 104 Degrees Fahrenheit |
Handling Environment Temperature | Between 50 Degrees Fahrenheit and 104 Degrees Fahrenheit |
Handling Environment Temperature | Between 50 Degrees Fahrenheit and 104 Degrees Fahrenheit |
Handling Environment Temperature | Between 50 Degrees Fahrenheit and 104 Degrees Fahrenheit |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00858058005085 [Primary] |
GS1 | 10858058005082 [Package] Contains: 00858058005085 Package: Outer carton [6 Units] In Commercial Distribution |
NUH | Stimulator, Nerve, Transcutaneous, Over-The-Counter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-05-23 |
Device Publish Date | 2018-04-23 |
10858058005082 | Neuromuscular Electrical Stimulation Device |
10858058005235 | Neuromuscular Electrical Stimulation Device |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
REVITIVE MEDIC 88351128 not registered Live/Pending |
Actegy Limited 2019-03-21 |