Primary Device ID | 18054655015413 |
NIH Device Record Key | 93d874b3-92bd-4ee3-8a12-94a7c13df79c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Spes Medica Subdermal Needle Electrodes |
Version Model Number | TT05MN4013D/15 |
Company DUNS | 514029771 |
Company Name | SPES MEDICA SRL |
Device Count | 20 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 | true |
RX Perscription | false |
OTC Over-The-Counter | false |