FDA UDI In Commercial Distribution 🇺🇸 United States

HIDREX USA

DI: 04250571300610 · Model: DVP1000 Package HF AL · HIDREX GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HIDREX USA
Primary DI
04250571300610
Version / Model
DVP1000 Package HF AL
Catalog Number
ION17110US
Company Name
HIDREX GmbH
Labeler DUNS
326742426
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-08
Public Version
3
Public Version Date
2022-11-09
Public Version Status
Update
Public Device Record Key
6affcc39-5416-47de-b144-d743bf9faedd

Device Description

HIDREX USA DVP1000 Iontophoresis Device Package Hand/Foot (Aluminum Electrode Plates, US Type A Plug)

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
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
17421 Hyperhidrosis iontophoresis system

Identifiers

Type ID
Primary 04250571300610

Customer Contacts

Phone
9999999999