FDA UDI In Commercial Distribution 🇺🇸 United States

Electrodes

DI: 00817377023118 · Model: 13-50000-0001 · DYMEDIX DIAGNOSTICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Electrodes
Primary DI
00817377023118
Version / Model
13-50000-0001
Company Name
DYMEDIX DIAGNOSTICS, INC.
Labeler DUNS
079976463
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-06
Public Version
1
Public Version Date
2021-07-14
Public Version Status
New
Public Device Record Key
727dfe25-e219-487c-9032-3eed1a1fa07d

Device Description

XM Movement Sensor

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
GXY Electrode, Cutaneous

GMDN Terms

Code Name
33843 Polysomnograph

Identifiers

Type ID
Package 10817377023115
Primary 00817377023118
Package 20817377023112

Premarket Submissions

Submission Number Supplement Number
K020468 000