FDA UDI In Commercial Distribution 🇺🇸 United States

Vive Precision

DI: 00810113572451 · Model: DMD1083BLU300 · VIVE HEALTH LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Vive Precision
Primary DI
00810113572451
Version / Model
DMD1083BLU300
Company Name
VIVE HEALTH LLC
Labeler DUNS
047025993
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-24
Public Version
1
Public Version Date
2023-09-01
Public Version Status
New
Public Device Record Key
9a63f1c9-9c90-43d1-ae0d-aa6ff5a6c199

Device Description

Easy-Twist Lancets (300PK)

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

GMDN Terms

Code Name
61578 Manual blood lancing device, single-use

Identifiers

Type ID
Package 10810113572458
Primary 00810113572451