FDA UDI Not in Commercial Distribution 🇺🇸 United States

NeuroTherm™

DI: 05415067022929 · Model: CLASSIC · NEUROTHERM, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NeuroTherm™
Primary DI
05415067022929
Version / Model
CLASSIC
Catalog Number
C-505-B-22
Company Name
NEUROTHERM, INC.
Labeler DUNS
124023552
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-14
Public Version
5
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
874352a1-62fd-4608-a177-c9172aa7f024
Distribution End Date
2018-04-05

Device Description

Radiofrequency Cannula-Curved Blunt

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GXI PROBE, RADIOFREQUENCY LESION

GMDN Terms

Code Name
58739 Percutaneous radio-frequency ablation probe cannula, single-use

Identifiers

Type ID
Package 15415067022926
Primary 05415067022929

Customer Contacts

Device Sizes

Type Value Unit Text
Needle Gauge 22 Gauge

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a cool, dry place; avoid exposure to extreme temperatures.