FDA UDI In Commercial Distribution 🇺🇸 United States

Nova

DI: 00385480487375 · Model: SUREFLEX · NOVA BIOMEDICAL CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
30

Basic Information

Brand Name
Nova
Primary DI
00385480487375
Version / Model
SUREFLEX
Catalog Number
48737
Company Name
NOVA BIOMEDICAL CORPORATION
Labeler DUNS
070617139
Distribution Status
In Commercial Distribution
Device Count in Pkg
30
Record Status
Published
Publish Date
2016-09-20
Public Version
3
Public Version Date
2019-08-09
Public Version Status
Update
Public Device Record Key
1b24b88e-8768-47fb-9695-652f1ea7c733

Device Description

Nova Sureflex 30 Lancets

Device Characteristics

Single Use
Yes
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
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NBW SYSTEM, TEST, BLOOD GLUCOSE, OVER THE COUNTER

GMDN Terms

Code Name
62538 Glucose monitoring system IVD, point-of-care

Identifiers

Type ID
Package 10385480487372
Primary 00385480487375
Unit of Use 00385489487376

Customer Contacts