Primary Device ID | 00852423006479 |
NIH Device Record Key | 9250c8d3-e005-4d9d-a320-dd40ab4ef16e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EMYO® |
Version Model Number | EMYO® 200S |
Catalog Number | EM200S |
Company DUNS | 625863568 |
Company Name | PROMETHEUS GROUP OF NEW HAMPSHIRE LIMITED, THE |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | true |
OTC Over-The-Counter | false |
Phone | 800-442-2325 |
info@theprogrp.com | |
Phone | 800-442-2325 |
info@theprogrp.com | |
Phone | 800-442-2325 |
info@theprogrp.com | |
Phone | 800-442-2325 |
info@theprogrp.com | |
Phone | 800-442-2325 |
info@theprogrp.com | |
Phone | 800-442-2325 |
info@theprogrp.com | |
Phone | 800-442-2325 |
info@theprogrp.com | |
Phone | 800-442-2325 |
info@theprogrp.com | |
Phone | 800-442-2325 |
info@theprogrp.com | |
Phone | 800-442-2325 |
info@theprogrp.com | |
Phone | 800-442-2325 |
info@theprogrp.com | |
Phone | 800-442-2325 |
info@theprogrp.com | |
Phone | 800-442-2325 |
info@theprogrp.com | |
Phone | 800-442-2325 |
info@theprogrp.com | |
Phone | 800-442-2325 |
info@theprogrp.com | |
Phone | 800-442-2325 |
info@theprogrp.com | |
Phone | 800-442-2325 |
info@theprogrp.com | |
Phone | 800-442-2325 |
info@theprogrp.com | |
Phone | 800-442-2325 |
info@theprogrp.com | |
Phone | 800-442-2325 |
info@theprogrp.com | |
Phone | 800-442-2325 |
info@theprogrp.com | |
Phone | 800-442-2325 |
info@theprogrp.com | |
Phone | 800-442-2325 |
info@theprogrp.com | |
Phone | 800-442-2325 |
info@theprogrp.com | |
Phone | 800-442-2325 |
info@theprogrp.com | |
Phone | 800-442-2325 |
info@theprogrp.com | |
Phone | 800-442-2325 |
info@theprogrp.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00852423006479 [Primary] |
HCC | Device, Biofeedback |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-09-08 |
Device Publish Date | 2021-08-31 |
00852423006455 | EMYO®100 is a Single Channel EMG System for Adult and Pediatric Pelvic Floor Rehabilitation |
00852423006448 | EMYO®200 is a Dual Channel EMG System for Adult and Pediatric Pelvic Floor Rehabilitation |
00852423006486 | EMYO®100S is a Single Channel EMG System for dysphagia rehabilitation |
00852423006479 | EMYO® 200S is a dual channel EMG System for dysphagia rehabilitation |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
EMYO 88407546 not registered Live/Pending |
The Prometheus Group of New Hampshire, Limited 2019-04-29 |
EMYO 87127134 not registered Live/Pending |
PregLem S.A. 2016-08-04 |
EMYO 79090739 4085736 Dead/Cancelled |
Richter Gedeon Nyrt. 2010-11-17 |