FDA UDI Not in Commercial Distribution 🇺🇸 United States

Nova Plus®

DI: 10707387566736 · Model: V2237-5 · 3M COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
Nova Plus®
Primary DI
10707387566736
Version / Model
V2237-5
Catalog Number
V2237-5
Company Name
3M COMPANY
Labeler DUNS
830016148
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2016-09-24
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
88e884f4-631e-439a-8b05-8bb271a99d51
Distribution End Date
2017-07-28

Device Description

Nova Plus® Foam Monitoring Electrode, 5/Bag, 200/Case, 24/Plt V2237-5

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DRX Electrode, electrocardiograph

GMDN Terms

Code Name
35035 Electrocardiographic electrode, single-use

Identifiers

Type ID
Package 50707387566734
Primary 10707387566736
Unit of Use 00707387566739

Customer Contacts