FDA UDI In Commercial Distribution 🇺🇸 United States

Venni / Biolight

DI: 00852503007174 · Model: E30 · VENNI INSTRUMENTS INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Venni / Biolight
Primary DI
00852503007174
Version / Model
E30
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
2021-03-10
Public Version Status
Update
Public Device Record Key
98a84c8a-1610-422f-9414-12f9f9f19663

Device Description

Venni / Biolight 3-channel EKG machine

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
DPS Electrocardiograph

GMDN Terms

Code Name
16231 Electrocardiograph, professional, multichannel

Identifiers

Type ID
Primary 00852503007174

Customer Contacts

Phone
888-822-5887

Premarket Submissions

Submission Number Supplement Number
K131858 000