Primary Device ID | NRP130 |
NIH Device Record Key | 3e50c36a-2d97-4f89-98a3-ed5d6d6209cc |
Commercial Distribution Discontinuation | 2023-07-12 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | NES Reprocessed 0.9mm RX Turbo Elite Laser Atherectomy Catheter |
Version Model Number | R-410-154 |
Company DUNS | 608625823 |
Company Name | NORTH EAST SCIENTIFIC INC |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 203-756-2111 |
matt@smarthealth-care.com | |
Phone | 203-756-2111 |
matt@smarthealth-care.com | |
Phone | 203-756-2111 |
matt@smarthealth-care.com | |
Phone | 203-756-2111 |
matt@smarthealth-care.com | |
Phone | 203-756-2111 |
matt@smarthealth-care.com | |
Phone | 203-756-2111 |
matt@smarthealth-care.com | |
Phone | 203-756-2111 |
matt@smarthealth-care.com | |
Phone | 203-756-2111 |
matt@smarthealth-care.com | |
Phone | 203-756-2111 |
matt@smarthealth-care.com | |
Phone | 203-756-2111 |
matt@smarthealth-care.com | |
Phone | 203-756-2111 |
matt@smarthealth-care.com | |
Phone | 203-756-2111 |
matt@smarthealth-care.com | |
Phone | 203-756-2111 |
matt@smarthealth-care.com | |
Phone | 203-756-2111 |
matt@smarthealth-care.com | |
Phone | 203-756-2111 |
matt@smarthealth-care.com | |
Phone | 203-756-2111 |
matt@smarthealth-care.com | |
Phone | 203-756-2111 |
matt@smarthealth-care.com | |
Phone | 203-756-2111 |
matt@smarthealth-care.com |
Catheter Working Length | 150 Centimeter |
Lumen/Inner Diameter | 0.014 Inch |
Guidewire Compatibility | 4 French |
Catheter Working Length | 150 Centimeter |
Lumen/Inner Diameter | 0.014 Inch |
Guidewire Compatibility | 4 French |
Catheter Working Length | 150 Centimeter |
Lumen/Inner Diameter | 0.014 Inch |
Guidewire Compatibility | 4 French |
Catheter Working Length | 150 Centimeter |
Lumen/Inner Diameter | 0.014 Inch |
Guidewire Compatibility | 4 French |
Catheter Working Length | 150 Centimeter |
Lumen/Inner Diameter | 0.014 Inch |
Guidewire Compatibility | 4 French |
Catheter Working Length | 150 Centimeter |
Lumen/Inner Diameter | 0.014 Inch |
Guidewire Compatibility | 4 French |
Catheter Working Length | 150 Centimeter |
Lumen/Inner Diameter | 0.014 Inch |
Guidewire Compatibility | 4 French |
Catheter Working Length | 150 Centimeter |
Lumen/Inner Diameter | 0.014 Inch |
Guidewire Compatibility | 4 French |
Catheter Working Length | 150 Centimeter |
Lumen/Inner Diameter | 0.014 Inch |
Guidewire Compatibility | 4 French |
Catheter Working Length | 150 Centimeter |
Lumen/Inner Diameter | 0.014 Inch |
Guidewire Compatibility | 4 French |
Catheter Working Length | 150 Centimeter |
Lumen/Inner Diameter | 0.014 Inch |
Guidewire Compatibility | 4 French |
Catheter Working Length | 150 Centimeter |
Lumen/Inner Diameter | 0.014 Inch |
Guidewire Compatibility | 4 French |
Catheter Working Length | 150 Centimeter |
Lumen/Inner Diameter | 0.014 Inch |
Guidewire Compatibility | 4 French |
Catheter Working Length | 150 Centimeter |
Lumen/Inner Diameter | 0.014 Inch |
Guidewire Compatibility | 4 French |
Catheter Working Length | 150 Centimeter |
Lumen/Inner Diameter | 0.014 Inch |
Guidewire Compatibility | 4 French |
Catheter Working Length | 150 Centimeter |
Lumen/Inner Diameter | 0.014 Inch |
Guidewire Compatibility | 4 French |
Catheter Working Length | 150 Centimeter |
Lumen/Inner Diameter | 0.014 Inch |
Guidewire Compatibility | 4 French |
Catheter Working Length | 150 Centimeter |
Lumen/Inner Diameter | 0.014 Inch |
Guidewire Compatibility | 4 French |
Device Issuing Agency | Device ID |
---|---|
HIBCC | NRP130 [Primary] |
QTF | Reprocessed Atherectomy Catheter |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2023-07-13 |
Device Publish Date | 2022-12-08 |
NRP130 | The device is the Phillips 0.9mm RX Turbo Elite Laser Atherectomy catheter that is reprocessed b |
B227NRP1300 | The device is the Phillips 0.9mm RX Turbo Elite Laser Atherectomy catheter that is reprocessed b |