FDA UDI In Commercial Distribution 🇺🇸 United States

Biolight

DI: 00852503007150 · Model: V6 · VENNI INSTRUMENTS INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Biolight
Primary DI
00852503007150
Version / Model
V6
Company Name
VENNI INSTRUMENTS INC.
Labeler DUNS
960516735
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-06
Public Version
5
Public Version Date
2021-11-10
Public Version Status
Update
Public Device Record Key
a6f0d067-bc6a-475c-aeea-b1c51d499c6a

Device Description

Biolight Vital Signs Monitor

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
MWI Monitor,Physiological,Patient(Without Arrhythmia Detection Or Alarms)

GMDN Terms

Code Name
33586 General-purpose multi-parameter bedside monitor

Identifiers

Type ID
Primary 00852503007150

Customer Contacts

Phone
888-822-5887