NES Reprocessed RF Stylet (RFS) R-RFS2-6-12

GUDID B227RRFS26120

NORTH EAST SCIENTIFIC INC

Tumour-therapy radio-frequency hyperthermia system applicator, intracorporeal Tumour-therapy radio-frequency hyperthermia system applicator, intracorporeal Tumour-therapy radio-frequency hyperthermia system applicator, intracorporeal Tumour-therapy radio-frequency hyperthermia system applicator, intracorporeal Tumour-therapy radio-frequency hyperthermia system applicator, intracorporeal Tumour-therapy radio-frequency hyperthermia system applicator, intracorporeal Tumour-therapy radio-frequency hyperthermia system applicator, intracorporeal Tumour-therapy radio-frequency hyperthermia system applicator, intracorporeal Tumour-therapy radio-frequency hyperthermia system applicator, intracorporeal Tumour-therapy radio-frequency hyperthermia system applicator, intracorporeal Tumour-therapy radio-frequency hyperthermia system applicator, intracorporeal Tumour-therapy radio-frequency hyperthermia system applicator, intracorporeal Tumour-therapy radio-frequency hyperthermia system applicator, intracorporeal Tumour-therapy radio-frequency hyperthermia system applicator, intracorporeal Tumour-therapy radio-frequency hyperthermia system applicator, intracorporeal Tumour-therapy radio-frequency hyperthermia system applicator, intracorporeal Tumour-therapy radio-frequency hyperthermia system applicator, intracorporeal Tumour-therapy radio-frequency hyperthermia system applicator, intracorporeal
Primary Device IDB227RRFS26120
NIH Device Record Key26095f90-fe51-4e02-98ff-e60b82977200
Commercial Distribution Discontinuation2030-11-24
Commercial Distribution StatusIn Commercial Distribution
Brand NameNES Reprocessed RF Stylet (RFS)
Version Model NumberR-RFS2-6-12
Catalog NumberR-RFS2-6-12
Company DUNS608625823
Company NameNORTH EAST SCIENTIFIC INC
Device Count1
DM Exempttrue
Pre-market Exemptfalse
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 Identifiers

Device Issuing AgencyDevice ID
HIBCCB227RRFS26120 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NUJElectrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-07-20
Device Publish Date2023-07-12

On-Brand Devices [NES Reprocessed RF Stylet (RFS)]

B227RRFS2612The device is the Covidien ClosureRFS Endovenous Radiofrequency (RF) Stylet that is reprocessed
B227RRFS26120R-RFS2-6-12

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.