FDA UDI In Commercial Distribution 🇺🇸 United States

Vive Precision

DI: 00818323022094 · Model: DMD1034WHT · VIVE HEALTH LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Vive Precision
Primary DI
00818323022094
Version / Model
DMD1034WHT
Company Name
VIVE HEALTH LLC
Labeler DUNS
047025993
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-02-01
Public Version
4
Public Version Date
2021-11-10
Public Version Status
Update
Public Device Record Key
002d7e11-50fc-4263-a81b-8d6ea77abffb

Device Description

Pulse Oximeter Bluetooth

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
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
45607 Pulse oximeter

Identifiers

Type ID
Package 10818323022091
Primary 00818323022094

Premarket Submissions

Submission Number Supplement Number
K170965 000