NeuroTherm™ SL-C1010-18

GUDID 15415067021738

NEUROTHERM, INC.

Radio-frequency ablation system probe cannula, single-use Percutaneous radio-frequency ablation system probe cannula, single-use Percutaneous radio-frequency ablation system probe cannula, single-use Percutaneous radio-frequency ablation system probe cannula, single-use Percutaneous radio-frequency ablation system probe cannula, single-use Percutaneous radio-frequency ablation system probe cannula, single-use Percutaneous radio-frequency ablation system probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use
Primary Device ID15415067021738
NIH Device Record Key40b83ca8-8add-4bdd-9b9e-ea2b545ddf56
Commercial Distribution StatusIn Commercial Distribution
Brand NameNeuroTherm™
Version Model NumberSL
Catalog NumberSL-C1010-18
Company DUNS124023552
Company NameNEUROTHERM, INC.
Device Count1
DM Exemptfalse
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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com

Device Dimensions

Needle Gauge18 Gauge
Needle Gauge18 Gauge
Needle Gauge18 Gauge
Needle Gauge18 Gauge
Needle Gauge18 Gauge
Needle Gauge18 Gauge
Needle Gauge18 Gauge
Needle Gauge18 Gauge
Needle Gauge18 Gauge
Needle Gauge18 Gauge
Needle Gauge18 Gauge
Needle Gauge18 Gauge
Needle Gauge18 Gauge
Needle Gauge18 Gauge
Needle Gauge18 Gauge
Needle Gauge18 Gauge
Needle Gauge18 Gauge
Needle Gauge18 Gauge
Needle Gauge18 Gauge
Needle Gauge18 Gauge
Needle Gauge18 Gauge

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry place, avoid extreme temperatures
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry place, avoid extreme temperatures
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry place, avoid extreme temperatures
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry place, avoid extreme temperatures
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry place, avoid extreme temperatures
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry place, avoid extreme temperatures
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry place, avoid extreme temperatures
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry place, avoid extreme temperatures
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry place, avoid extreme temperatures
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry place, avoid extreme temperatures
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry place, avoid extreme temperatures
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry place, avoid extreme temperatures
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry place, avoid extreme temperatures
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry place, avoid extreme temperatures
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry place, avoid extreme temperatures
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry place, avoid extreme temperatures
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry place, avoid extreme temperatures
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry place, avoid extreme temperatures
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry place, avoid extreme temperatures
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry place, avoid extreme temperatures
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dry place, avoid extreme temperatures

Device Identifiers

Device Issuing AgencyDevice ID
GS105415067021731 [Primary]
GS115415067021738 [Package]
Contains: 05415067021731
Package: [10 Units]
In Commercial Distribution

FDA Product Code

GXIPROBE, RADIOFREQUENCY LESION

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2015-07-31

On-Brand Devices [NeuroTherm™]

05415067026576PodiaTherm Disposable Kit
05415067023629RF-DGP-S
05415067023612Grounding Pad
15415067022926Radiofrequency Cannula-Curved Blunt
15415067022919SL
15415067022452CLASSIC
15415067022445CLASSIC
15415067022438CLASSIC
15415067022407CLASSIC
15415067022391RFDEUK-5
15415067022360RFDEUK-20
15415067022346RFDEUK-15
15415067022315Disposable Radiofrequency Electrode
15415067022292CLASSIC
15415067022285CLASSIC
15415067022261CLASSIC
15415067022247Radiofrequency Cannula - Straight
15415067022230CLASSIC
15415067022193CLASSIC
15415067022179CLASSIC
15415067022155CLASSIC
15415067022131CLASSIC
15415067022124CLASSIC
15415067022117CLASSIC
15415067022100CLASSIC
15415067022094CLASSIC
15415067022087CLASSIC
15415067022070CLASSIC
15415067022063CLASSIC
15415067022056CLASSIC
15415067022049CLASSIC
15415067022032CLASSIC
15415067022025CLASSIC
15415067022018CLASSIC
15415067022001CLASSIC
15415067021998CLASSIC
15415067021981CLASSIC
15415067021974CLASSIC
15415067021967CLASSIC
15415067021950CLASSIC
15415067021943CLASSIC
15415067021936CLASSIC
15415067021929CLASSIC
15415067021912Radiofrequency Cannula - Curved
15415067021905Radiofrequency Cannula - Curved
15415067021899Radiofrequency Cannula - Curved
15415067021882Radiofrequency Cannula - Curved
15415067021875Radiofrequency Cannula - Curved
15415067021868Radiofrequency Cannula - Straight
15415067021851Radiofrequency Cannula - Straight

Trademark Results [NeuroTherm]

Mark Image

Registration | Serial
Company
Trademark
Application Date
NEUROTHERM
NEUROTHERM
76063816 2575296 Live/Registered
NEUROTHERM INC.
2000-06-06

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