Primary Device ID | 05060488570971 |
NIH Device Record Key | 27113833-abcd-4052-9054-343a6efdc580 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Protekt Titanium Adhesive Pre-Gelled Electrode for TENS - Round 2" |
Version Model Number | PMTENSEL3 |
Catalog Number | PMTENSEL3 |
Company DUNS | 078582655 |
Company Name | PROACTIVE MEDICAL PRODUCTS, LLC |
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 | true |
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 | false |
Phone | +1 855 237 7622 |
sales@proactivemedical.com | |
Phone | +1 855 237 7622 |
sales@proactivemedical.com | |
Phone | +1 855 237 7622 |
sales@proactivemedical.com | |
Phone | +1 855 237 7622 |
sales@proactivemedical.com | |
Phone | +1 855 237 7622 |
sales@proactivemedical.com | |
Phone | +1 855 237 7622 |
sales@proactivemedical.com | |
Phone | +1 855 237 7622 |
sales@proactivemedical.com | |
Phone | +1 855 237 7622 |
sales@proactivemedical.com | |
Phone | +1 855 237 7622 |
sales@proactivemedical.com | |
Phone | +1 855 237 7622 |
sales@proactivemedical.com | |
Phone | +1 855 237 7622 |
sales@proactivemedical.com | |
Phone | +1 855 237 7622 |
sales@proactivemedical.com | |
Phone | +1 855 237 7622 |
sales@proactivemedical.com | |
Phone | +1 855 237 7622 |
sales@proactivemedical.com | |
Phone | +1 855 237 7622 |
sales@proactivemedical.com | |
Phone | +1 855 237 7622 |
sales@proactivemedical.com | |
Phone | +1 855 237 7622 |
sales@proactivemedical.com |
Length | 4 Inch |
Height | 1 Inch |
Width | 6 Inch |
Length | 4 Inch |
Height | 1 Inch |
Width | 6 Inch |
Length | 4 Inch |
Height | 1 Inch |
Width | 6 Inch |
Length | 4 Inch |
Height | 1 Inch |
Width | 6 Inch |
Length | 4 Inch |
Height | 1 Inch |
Width | 6 Inch |
Length | 4 Inch |
Height | 1 Inch |
Width | 6 Inch |
Length | 4 Inch |
Height | 1 Inch |
Width | 6 Inch |
Length | 4 Inch |
Height | 1 Inch |
Width | 6 Inch |
Length | 4 Inch |
Height | 1 Inch |
Width | 6 Inch |
Length | 4 Inch |
Height | 1 Inch |
Width | 6 Inch |
Length | 4 Inch |
Height | 1 Inch |
Width | 6 Inch |
Length | 4 Inch |
Height | 1 Inch |
Width | 6 Inch |
Length | 4 Inch |
Height | 1 Inch |
Width | 6 Inch |
Length | 4 Inch |
Height | 1 Inch |
Width | 6 Inch |
Length | 4 Inch |
Height | 1 Inch |
Width | 6 Inch |
Length | 4 Inch |
Height | 1 Inch |
Width | 6 Inch |
Length | 4 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05060488570971 [Primary] |
GXY | Electrode, Cutaneous |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-01-09 |
Device Publish Date | 2020-01-01 |
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