FDA UDI In Commercial Distribution 🇺🇸 United States

Electrolite

DI: 10609960000173 · Model: 26200 · DERMATOLOGIC LAB AND SUPPLY, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Electrolite
Primary DI
10609960000173
Version / Model
26200
Company Name
DERMATOLOGIC LAB AND SUPPLY, INC.
Labeler DUNS
021628771
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2016-05-13
Public Version
3
Public Version Date
2019-02-07
Public Version Status
Update
Public Device Record Key
bba28309-ca55-430e-95e0-3b118cc03f65

Device Description

ELECTROLITE ELECTRODES, DISPOSBL,NONSTERILE,BX/100

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
No
Has Donation ID
Yes

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
61874 Open-surgery electrosurgical electrode, monopolar, single-use

Identifiers

Type ID
Primary 10609960000173
Unit of Use 00609960000176
Package 20609960000170