FDA UDI In Commercial Distribution 🇺🇸 United States

Ionto Plus Medium Electrodes

DI: 00092237901762 · Model: 201-449 · COMPASS HEALTH BRANDS CORP.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
2

Basic Information

Brand Name
Ionto Plus Medium Electrodes
Primary DI
00092237901762
Version / Model
201-449
Company Name
COMPASS HEALTH BRANDS CORP.
Labeler DUNS
827221698
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2018-09-26
Public Version
2
Public Version Date
2023-08-07
Public Version Status
Update
Public Device Record Key
a3f3527c-30bf-4248-84f6-a47b8506c662

Device Description

Iontophoresis Drug Delivery Medium Kit Electrodes - 2.5cc, 4mA-min incl. buffered return 3.25" x 3.25"

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
EGJ Device, Iontophoresis, Other Uses

GMDN Terms

Code Name
45141 Drug-delivery iontophoresis patch

Identifiers

Type ID
Package 80092237901768
Package 30092237901763
Primary 00092237901762
Unit of Use 01092237901761

Customer Contacts

Phone
800-376-7263