Primary Device ID | 00816864020098 |
NIH Device Record Key | 7f746082-20d2-4fce-ba1e-68e0f2611a79 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sys*Stim 208, one channel |
Version Model Number | ME 208 |
Catalog Number | ME 208 |
Company DUNS | 008513913 |
Company Name | METTLER ELECTRONICS CORP. |
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 | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(714)533-2221 |
service@mettlerelectronics.com | |
Phone | +1(714)533-2221 |
service@mettlerelectronics.com | |
Phone | +1(714)533-2221 |
service@mettlerelectronics.com |
Weight | 1.4 Pound |
Weight | 1.4 Pound |
Weight | 1.4 Pound |
Special Storage Condition, Specify | Between 0 and 0 *No |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00816864020098 [Primary] |
GZJ | STIMULATOR, NERVE, TRANSCUTANEOUS, FOR PAIN RELIEF |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-05-23 |
Device Publish Date | 2016-09-15 |
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