InnoHaus Art.- No. 642.74
GUDID 20853879007816
Digital TENS Device
BEURER NORTH AMERICA, L.P.
Transcutaneous electrical stimulation electrode Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use| Primary Device ID | 20853879007816 |
| NIH Device Record Key | b54d7939-e01f-4189-9092-f77a3270f993 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | InnoHaus |
| Version Model Number | AEM44 |
| Catalog Number | Art.- No. 642.74 |
| Company DUNS | 078497467 |
| Company Name | BEURER NORTH AMERICA, L.P. |
| 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 | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | true |
Customer Support Contacts
| Phone | 1-800-536-0366 |
| info@beurer.com | |
| Phone | 1-800-536-0366 |
| info@beurer.com | |
| Phone | 1-800-536-0366 |
| info@beurer.com | |
| Phone | 1-800-536-0366 |
| info@beurer.com | |
| Phone | 1-800-536-0366 |
| info@beurer.com | |
| Phone | 1-800-536-0366 |
| info@beurer.com | |
| Phone | 1-800-536-0366 |
| info@beurer.com | |
| Phone | 1-800-536-0366 |
| info@beurer.com | |
| Phone | 1-800-536-0366 |
| info@beurer.com | |
| Phone | 1-800-536-0366 |
| info@beurer.com | |
| Phone | 1-800-536-0366 |
| info@beurer.com | |
| Phone | 1-800-536-0366 |
| info@beurer.com | |
| Phone | 1-800-536-0366 |
| info@beurer.com | |
| Phone | 1-800-536-0366 |
| info@beurer.com | |
| Phone | 1-800-536-0366 |
| info@beurer.com | |
| Phone | 1-800-536-0366 |
| info@beurer.com | |
| Phone | 1-800-536-0366 |
| info@beurer.com | |
| Phone | 1-800-536-0366 |
| info@beurer.com | |
| Phone | 1-800-536-0366 |
| info@beurer.com | |
| Phone | 1-800-536-0366 |
| info@beurer.com | |
| Phone | 1-800-536-0366 |
| info@beurer.com | |
| Phone | 1-800-536-0366 |
| info@beurer.com | |
| Phone | 1-800-536-0366 |
| info@beurer.com | |
| Phone | 1-800-536-0366 |
| info@beurer.com | |
| Phone | 1-800-536-0366 |
| info@beurer.com | |
| Phone | 1-800-536-0366 |
| info@beurer.com | |
| Phone | 1-800-536-0366 |
| info@beurer.com | |
| Phone | 1-800-536-0366 |
| info@beurer.com | |
| Phone | 1-800-536-0366 |
| info@beurer.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00853879007812 [Primary] |
| GS1 | 10853879007819 [Package] Contains: 00853879007812 Package: Inner Pack [4 Units] In Commercial Distribution |
| GS1 | 20853879007816 [Package] Contains: 10853879007819 Package: Case Pack [6 Units] In Commercial Distribution |
FDA Product Code
| NUH | Stimulator, Nerve, Transcutaneous, Over-The-Counter |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-10-23 |
| Device Publish Date | 2018-09-10 |
On-Brand Devices [InnoHaus]
| 20853879007953 | IR Ear Thermometer |
| 20853879007847 | Wrist Blood Pressure Monitor |
| 10853879007826 | Blood Pressure Monitor with Universal Cuff (22 - 42 cm) |
| 20853879007816 | Digital TENS Device |
| 10853879007796 | Body Fat Scale |
Trademark Results [InnoHaus]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 INNOHAUS 88065107 not registered Live/Pending |
BEURER GMBH 2018-08-03 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.