FDA UDI In Commercial Distribution 🇺🇸 United States

PhysioFlow

DI: 15060441917536 · Model: HTFS50PF · NISSHA MEDICAL TECHNOLOGIES LTD
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
7

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Basic Information

Brand Name
PhysioFlow
Primary DI
15060441917536
Version / Model
HTFS50PF
Catalog Number
4012871C
Company Name
NISSHA MEDICAL TECHNOLOGIES LTD
Labeler DUNS
671405566
Distribution Status
In Commercial Distribution
Device Count in Pkg
7
Record Status
Published
Publish Date
2020-05-06
Public Version
1
Public Version Date
2020-05-14
Public Version Status
New
Public Device Record Key
a1014d40-c0af-402e-a111-6ffdb96a0037

Device Description

Stress Test & Holter ECG Electrode

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
Yes
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 35060441917530
Primary 15060441917536
Package 55060441917534
Unit of Use 05060441917539

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 40 Degrees Celsius