Primary Device ID | 08056446900635 |
NIH Device Record Key | dc99939b-febb-426c-a9b0-3ccc0bfbe04d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Circular Coil 90 mm air cooled |
Version Model Number | B9621086006 |
Company DUNS | 339182263 |
Company Name | EB NEURO SPA |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +390554565111 |
info@ebneuro.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08056446900635 [Primary] |
GWF | Stimulator, Electrical, Evoked Response |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-06-03 |
Device Publish Date | 2019-05-24 |
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