FDA UDI In Commercial Distribution 🇺🇸 United States

Everion+ System

DI: 08885018690007 · Model: EVRPLUS-G · BIOFOURMIS SINGAPORE PTE. LTD.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Everion+ System
Primary DI
08885018690007
Version / Model
EVRPLUS-G
Company Name
BIOFOURMIS SINGAPORE PTE. LTD.
Labeler DUNS
659253421
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-03-22
Public Version
1
Public Version Date
2023-03-30
Public Version Status
New
Public Device Record Key
50865a7c-eae1-4d97-aa67-e8de36953d93

Device Description

Everion+ System

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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
MSX System, Network And Communication, Physiological Monitors

GMDN Terms

Code Name
12391 Wearable multiple physiological parameter recorder, reusable

Identifiers

Type ID
Primary 08885018690007

Premarket Submissions

Submission Number Supplement Number
K213863 000