FDA UDI In Commercial Distribution 🇺🇸 United States

VIRTUOX

DI: 06942820462115 · Model: VPOD VITAL PRO · Beijing Choice Electronic Technology Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VIRTUOX
Primary DI
06942820462115
Version / Model
VPOD VITAL PRO
Company Name
Beijing Choice Electronic Technology Co., Ltd.
Labeler DUNS
526882823
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-10-20
Public Version
1
Public Version Date
2020-10-28
Public Version Status
New
Public Device Record Key
11896ac0-1d7a-48f5-8c27-cd372e099107

Device Description

VIRTUOX Vital Sign Monitor VPOD VITAL PRO

Device Characteristics

Single Use
No
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
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
DQA Oximeter

GMDN Terms

Code Name
17148 Pulse oximeter, line-powered

Identifiers

Type ID
Primary 06942820462115