Primary Device ID | 00643169498051 |
NIH Device Record Key | dae23931-f00b-4be5-b1e3-b670076a41e0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NeuroPEN |
Version Model Number | 3220-001 |
Company DUNS | 089055867 |
Company Name | MEDTRONIC PS MEDICAL, 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 | false |
Manufacturing Date | false |
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(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00643169498051 [Primary] |
GWG | ENDOSCOPE, NEUROLOGICAL |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00643169498051]
Moist Heat or Steam Sterilization
[00643169498051]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-06-13 |
00613994908490 | NEUROPEN 2120-035 15MM 19CM DF |
00613994840233 | NEUROPEN 2120-025 15MM 15.5 DF .045 |
00643169498051 | FORCEPS 3220-001 BIOPSY 3MM L 28.5CM |
00721902879784 | NEUROPEN 27769 W/NO EPOXY OVER END |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
NEUROPEN 75292296 2215863 Live/Registered |
Owen Mumford Limited 1997-05-15 |
NEUROPEN 75082984 2037241 Dead/Cancelled |
Clarus Medical Systems, Inc. 1996-04-03 |