FDA UDI Not in Commercial Distribution 🇺🇸 United States

NeuroTherm™

DI: 05415067023629 · Model: RF-DGP-S · NEUROTHERM, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NeuroTherm™
Primary DI
05415067023629
Version / Model
RF-DGP-S
Catalog Number
RF-DGP-S
Company Name
NEUROTHERM, INC.
Labeler DUNS
124023552
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-07-31
Public Version
4
Public Version Date
2021-02-25
Public Version Status
Update
Public Device Record Key
f0b4affc-70f2-45cd-a265-4e7daeb3f760
Distribution End Date
2020-04-02

Device Description

Grounding Pad

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
58494 Electrosurgical return electrode, single-use

Identifiers

Type ID
Primary 05415067023629
Package 15415067023626

Customer Contacts