FDA UDI In Commercial Distribution 🇺🇸 United States

Corpuls

DI: 15060842920234 · Model: 1019CO · NISSHA MEDICAL TECHNOLOGIES LTD
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
50

Basic Information

Brand Name
Corpuls
Primary DI
15060842920234
Version / Model
1019CO
Catalog Number
19101.19
Company Name
NISSHA MEDICAL TECHNOLOGIES LTD
Labeler DUNS
671405566
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2025-02-18
Public Version
1
Public Version Date
2025-02-26
Public Version Status
New
Public Device Record Key
8ca6a48f-ddd1-4d69-ba9e-75053c66a707

Device Description

ECG Electrode

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DRX Electrode, Electrocardiograph

GMDN Terms

Code Name
35035 Electrocardiographic electrode, single-use

Identifiers

Type ID
Package 35060842920238
Primary 15060842920234
Package 55060842920232
Unit of Use 05060842920237

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 40 Degrees Celsius
Type
Special Storage Condition, Specify
Special Conditions
Keep Dry
Type
Special Storage Condition, Specify
Special Conditions
Keep out of direct sunlight