Primary Device ID | 00852423006325 |
NIH Device Record Key | 2539c73f-ec79-4e12-91a9-093ec527b00b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Quickscan |
Version Model Number | N/A |
Catalog Number | QSBU |
Company DUNS | 625863568 |
Company Name | PROMETHEUS GROUP OF NEW HAMPSHIRE LIMITED, THE |
Device Count | 1 |
DM Exempt | true |
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 | true |
OTC Over-The-Counter | false |
Phone | 1.800.442.2325 |
info@theprogrp.com | |
Phone | 1.800.442.2325 |
info@theprogrp.com | |
Phone | 1.800.442.2325 |
info@theprogrp.com | |
Phone | 1.800.442.2325 |
info@theprogrp.com | |
Phone | 1.800.442.2325 |
info@theprogrp.com | |
Phone | 1.800.442.2325 |
info@theprogrp.com | |
Phone | 1.800.442.2325 |
info@theprogrp.com | |
Phone | 1.800.442.2325 |
info@theprogrp.com | |
Phone | 1.800.442.2325 |
info@theprogrp.com | |
Phone | 1.800.442.2325 |
info@theprogrp.com | |
Phone | 1.800.442.2325 |
info@theprogrp.com | |
Phone | 1.800.442.2325 |
info@theprogrp.com | |
Phone | 1.800.442.2325 |
info@theprogrp.com | |
Phone | 1.800.442.2325 |
info@theprogrp.com | |
Phone | 1.800.442.2325 |
info@theprogrp.com | |
Phone | 1.800.442.2325 |
info@theprogrp.com | |
Phone | 1.800.442.2325 |
info@theprogrp.com | |
Phone | 1.800.442.2325 |
info@theprogrp.com | |
Phone | 1.800.442.2325 |
info@theprogrp.com | |
Phone | 1.800.442.2325 |
info@theprogrp.com | |
Phone | 1.800.442.2325 |
info@theprogrp.com | |
Phone | 1.800.442.2325 |
info@theprogrp.com | |
Phone | 1.800.442.2325 |
info@theprogrp.com | |
Phone | 1.800.442.2325 |
info@theprogrp.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00852423006325 [Primary] |
IYO | System, Imaging, Pulsed Echo, Ultrasonic |
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 | 2016-09-30 |
00852423006479 - EMYO® | 2021-09-08 EMYO® 200S is a dual channel EMG System for dysphagia rehabilitation |
00852423006486 - EMYO® | 2021-09-08 EMYO®100S is a Single Channel EMG System for dysphagia rehabilitation |
00852423006462 - Morpheus® | 2021-07-30 Morpheus® Transperineal Ultrasound Imaging |
00852423006448 - EMYO® | 2020-07-01 EMYO®200 is a Dual Channel EMG System for Adult and Pediatric Pelvic Floor Rehabilitation |
00852423006455 - EMYO® | 2020-07-01 EMYO®100 is a Single Channel EMG System for Adult and Pediatric Pelvic Floor Rehabilitation |
00852423006431 - TELESIS® | 2019-10-11 9250-ST Telesis® ST Software for Speech Therapy MR Series |
00852423006004 - Morpheus | 2019-10-07 Morpheus® Control Module |
00852423006011 - Pathway | 2018-12-24 Pathway® CTS 2000 |