Primary Device ID | 05415067021267 |
NIH Device Record Key | f1fff0e4-3d55-4882-b909-06adecaddc5f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NeuroTherm™ |
Version Model Number | AC-B-NT |
Catalog Number | AC-B-NT |
Company DUNS | 124023552 |
Company Name | NEUROTHERM, INC. |
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 | true |
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(855)478-5833 |
customerservice@sjm.com |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool dry place; avoid exposure to extreme temperatures. |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05415067021267 [Primary] |
IKD | CABLE, ELECTRODE |
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 | 2016-09-09 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
NEUROTHERM 76063816 2575296 Live/Registered |
NEUROTHERM INC. 2000-06-06 |