FDA UDI In Commercial Distribution 🇺🇸 United States

physIQ Patient Kit

DI: 00850023120069 · Model: Model I · PHYSIQ, INC
Product Codes
0
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
physIQ Patient Kit
Primary DI
00850023120069
Version / Model
Model I
Company Name
PHYSIQ, INC
Labeler DUNS
079107007
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-26
Public Version
1
Public Version Date
2021-08-03
Public Version Status
New
Public Device Record Key
f606ab40-5f91-45a3-8766-c180d00c9459

Device Description

physIQ convenience kit including mobile relay device pre-loaded with physIQ monitoring software, biosensors, and skin preparation materials.

Device Characteristics

Single Use
Yes
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
MR Unsafe
Direct Marking Exempt
Yes
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

GMDN Terms

Code Name
31733 Electrocardiography telemetric monitoring system

Identifiers

Type ID
Primary 00850023120069

Customer Contacts