NeuroBlate Optic SideFire® Laser Probe NBP-201-01

GUDID 00816589020908

3.3mm Directional Laser Probe

MONTERIS MEDICAL INC

MRI-guided laser interstitial thermal therapy system beam guide
Primary Device ID00816589020908
NIH Device Record Key29d0ddf1-352c-4f1e-baaf-23d79a8139d6
Commercial Distribution StatusIn Commercial Distribution
Brand NameNeuroBlate Optic SideFire® Laser Probe
Version Model Number20891-2
Catalog NumberNBP-201-01
Company DUNS021415875
Company NameMONTERIS MEDICAL INC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(866)799-7655
Emailgglaser@monteris.com
Phone+1(866)799-7655
Emailgglaser@monteris.com
Phone+1(866)799-7655
Emailgglaser@monteris.com

Device Dimensions

Device Size Text, specify0
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Device Identifiers

Device Issuing AgencyDevice ID
GS100816589020908 [Primary]

FDA Product Code

GEXPowered laser surgical instrument

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-11-19
Device Publish Date2018-10-17

On-Brand Devices [NeuroBlate Optic SideFire® Laser Probe]

008165890209393.3mm Directional Laser Probe
008165890209223.3mm Directional Laser Probe
008165890209153.3mm Directional Laser Probe
008165890209083.3mm Directional Laser Probe
008165890208923.3mm Directional Laser Probe
008165890208853.3mm Directional Laser Probe
008165890208783.3mm Directional Laser Probe

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