Primary Device ID | 00855547005175 |
NIH Device Record Key | f2a9d6f9-80dc-4ddc-bea6-de4f6a7610fd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ferrule Kit |
Version Model Number | F-01-K |
Company DUNS | 123369238 |
Company Name | Neuropace, Inc. |
Device Count | 1 |
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 | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | true |
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(866)726-3876 |
customerservice@neuropace.com |
Storage Environment Temperature | Between -10 Degrees Celsius and 60 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00855547005175 [Primary] |
PFN | Implanted brain stimulator for epilepsy |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-03-04 |
Device Publish Date | 2014-09-24 |
00855547005175 | The Ferrule package contains 1 Ferrule, 1 Ferrule Clamp and 1 Torque Driver. |
00855547005373 | The Ferrule package contains 1 Ferrule, 1 Ferrule Clamp and 1 Torque Driver. |