Primary Device ID | 00702173131887 |
NIH Device Record Key | bac77943-cc5a-4d84-a9dc-86f26f32a618 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Surgical Probe, Monopolar w/Protected Plug |
Version Model Number | 3188 |
Company DUNS | 006196604 |
Company Name | WR MEDICAL ELECTRONICS CO INC |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | 651-604-8400 |
info@wrmed.com | |
Phone | 651-604-8400 |
info@wrmed.com | |
Phone | 651-604-8400 |
info@wrmed.com | |
Phone | 651-604-8400 |
info@wrmed.com | |
Phone | 651-604-8400 |
info@wrmed.com | |
Phone | 651-604-8400 |
info@wrmed.com | |
Phone | 651-604-8400 |
info@wrmed.com | |
Phone | 651-604-8400 |
info@wrmed.com | |
Phone | 651-604-8400 |
info@wrmed.com | |
Phone | 651-604-8400 |
info@wrmed.com | |
Phone | 651-604-8400 |
info@wrmed.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00702173131887 [Primary] |
ETN | Stimulator, Nerve |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-08-29 |
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00702173151915 - Meridian™ Iontophoretic Drug Delivery Electrode | 2018-07-06 |
00702173152929 - Meridian™ Iontophoretic Drug Delivery Electrode | 2018-07-06 |
00702173155920 - Iontophor®-II | 2018-07-06 |