FDA UDI Not in Commercial Distribution 🇺🇸 United States

SideFire® Directional Laser Probe

DI: 00816589020786 · Model: 20368-4 · MONTERIS MEDICAL INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SideFire® Directional Laser Probe
Primary DI
00816589020786
Version / Model
20368-4
Catalog Number
NBP-401-01
Company Name
MONTERIS MEDICAL INC
Labeler DUNS
021415875
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-10-25
Public Version
3
Public Version Date
2018-10-18
Public Version Status
Update
Public Device Record Key
f888c8f8-4e5e-42a3-ba68-1ea39c8b813f
Distribution End Date
2018-10-17

Device Description

3.3mm Directional Laser Probe

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GEX Powered Laser Surgical Instrument

GMDN Terms

Code Name
62268 MRI-guided laser interstitial thermal therapy system beam guide

Identifiers

Type ID
Primary 00816589020786

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Size 4
Outer Diameter 3.3 Millimeter