NES Reprocessed 0.9mm RX Turbo Elite Laser Atherectomy Catheter

GUDID NRP130

The device is the Phillips 0.9mm RX Turbo Elite Laser Atherectomy catheter that is reprocessed by Northeast Scientific, Inc. (NES).

NORTH EAST SCIENTIFIC INC

Atherectomy laser system beam guide-catheter, peripheral Atherectomy laser system beam guide-catheter, peripheral Atherectomy laser system beam guide-catheter, peripheral Atherectomy laser system beam guide-catheter, peripheral Atherectomy laser system beam guide-catheter, peripheral Atherectomy laser system beam guide-catheter, peripheral Atherectomy laser system beam guide-catheter, peripheral Atherectomy laser system beam guide-catheter, peripheral Atherectomy laser system beam guide-catheter, peripheral Atherectomy laser system beam guide-catheter, peripheral Atherectomy laser system beam guide-catheter, peripheral Atherectomy laser system beam guide-catheter, peripheral Atherectomy laser system beam guide-catheter, peripheral Atherectomy laser system beam guide-catheter, peripheral Atherectomy laser system beam guide-catheter, peripheral Atherectomy laser system beam guide-catheter, peripheral Atherectomy laser system beam guide-catheter, peripheral Atherectomy laser system beam guide-catheter, peripheral
Primary Device IDNRP130
NIH Device Record Key3e50c36a-2d97-4f89-98a3-ed5d6d6209cc
Commercial Distribution Discontinuation2023-07-12
Commercial Distribution StatusNot in Commercial Distribution
Brand NameNES Reprocessed 0.9mm RX Turbo Elite Laser Atherectomy Catheter
Version Model NumberR-410-154
Company DUNS608625823
Company NameNORTH EAST SCIENTIFIC INC
Device Count1
DM Exempttrue
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone203-756-2111
Emailmatt@smarthealth-care.com
Phone203-756-2111
Emailmatt@smarthealth-care.com
Phone203-756-2111
Emailmatt@smarthealth-care.com
Phone203-756-2111
Emailmatt@smarthealth-care.com
Phone203-756-2111
Emailmatt@smarthealth-care.com
Phone203-756-2111
Emailmatt@smarthealth-care.com
Phone203-756-2111
Emailmatt@smarthealth-care.com
Phone203-756-2111
Emailmatt@smarthealth-care.com
Phone203-756-2111
Emailmatt@smarthealth-care.com
Phone203-756-2111
Emailmatt@smarthealth-care.com
Phone203-756-2111
Emailmatt@smarthealth-care.com
Phone203-756-2111
Emailmatt@smarthealth-care.com
Phone203-756-2111
Emailmatt@smarthealth-care.com
Phone203-756-2111
Emailmatt@smarthealth-care.com
Phone203-756-2111
Emailmatt@smarthealth-care.com
Phone203-756-2111
Emailmatt@smarthealth-care.com
Phone203-756-2111
Emailmatt@smarthealth-care.com
Phone203-756-2111
Emailmatt@smarthealth-care.com

Device Dimensions

Catheter Working Length150 Centimeter
Lumen/Inner Diameter0.014 Inch
Guidewire Compatibility4 French
Catheter Working Length150 Centimeter
Lumen/Inner Diameter0.014 Inch
Guidewire Compatibility4 French
Catheter Working Length150 Centimeter
Lumen/Inner Diameter0.014 Inch
Guidewire Compatibility4 French
Catheter Working Length150 Centimeter
Lumen/Inner Diameter0.014 Inch
Guidewire Compatibility4 French
Catheter Working Length150 Centimeter
Lumen/Inner Diameter0.014 Inch
Guidewire Compatibility4 French
Catheter Working Length150 Centimeter
Lumen/Inner Diameter0.014 Inch
Guidewire Compatibility4 French
Catheter Working Length150 Centimeter
Lumen/Inner Diameter0.014 Inch
Guidewire Compatibility4 French
Catheter Working Length150 Centimeter
Lumen/Inner Diameter0.014 Inch
Guidewire Compatibility4 French
Catheter Working Length150 Centimeter
Lumen/Inner Diameter0.014 Inch
Guidewire Compatibility4 French
Catheter Working Length150 Centimeter
Lumen/Inner Diameter0.014 Inch
Guidewire Compatibility4 French
Catheter Working Length150 Centimeter
Lumen/Inner Diameter0.014 Inch
Guidewire Compatibility4 French
Catheter Working Length150 Centimeter
Lumen/Inner Diameter0.014 Inch
Guidewire Compatibility4 French
Catheter Working Length150 Centimeter
Lumen/Inner Diameter0.014 Inch
Guidewire Compatibility4 French
Catheter Working Length150 Centimeter
Lumen/Inner Diameter0.014 Inch
Guidewire Compatibility4 French
Catheter Working Length150 Centimeter
Lumen/Inner Diameter0.014 Inch
Guidewire Compatibility4 French
Catheter Working Length150 Centimeter
Lumen/Inner Diameter0.014 Inch
Guidewire Compatibility4 French
Catheter Working Length150 Centimeter
Lumen/Inner Diameter0.014 Inch
Guidewire Compatibility4 French
Catheter Working Length150 Centimeter
Lumen/Inner Diameter0.014 Inch
Guidewire Compatibility4 French

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCNRP130 [Primary]

FDA Product Code

QTFReprocessed Atherectomy Catheter

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2023-07-13
Device Publish Date2022-12-08

On-Brand Devices [NES Reprocessed 0.9mm RX Turbo Elite Laser Atherectomy Catheter]

NRP130The device is the Phillips 0.9mm RX Turbo Elite Laser Atherectomy catheter that is reprocessed b
B227NRP1300The device is the Phillips 0.9mm RX Turbo Elite Laser Atherectomy catheter that is reprocessed b
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