FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 06970341674724 · Model: NA · GMDASZ manufacturing Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
06970341674724
Version / Model
NA
Company Name
GMDASZ manufacturing Co., Ltd.
Labeler DUNS
529401134
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-10-27
Public Version
4
Public Version Date
2021-02-19
Public Version Status
Update
Public Device Record Key
b64309f1-ed59-4225-a83a-e307be246bc4

Device Description

electrode pad, CWN2204, 19*35mm, rect.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
Yes
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
GXY Electrode, Cutaneous

GMDN Terms

Code Name
35995 Transcutaneous electrical stimulation electrode, single-use

Identifiers

Type ID
Package 06970341677558
Primary 06970341674724

Premarket Submissions

Submission Number Supplement Number
K160138 000