FDA UDI In Commercial Distribution 🇺🇸 United States

TRUEplus

DI: 00011822741125 · Model: Rite Aid TRUEplus Lancets · TRIVIDIA HEALTH, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
TRUEplus
Primary DI
00011822741125
Version / Model
Rite Aid TRUEplus Lancets
Catalog Number
S1066DB30-100
Company Name
TRIVIDIA HEALTH, INC.
Labeler DUNS
151810868
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2020-10-27
Public Version
2
Public Version Date
2022-12-28
Public Version Status
Update
Public Device Record Key
50f41ad3-d1b5-4628-837b-ca39c7db2a94

Device Description

Rite Aid TRUEplus 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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
QRK Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature

GMDN Terms

Code Name
45142 Blood lancing device tip

Identifiers

Type ID
Package 10011822741122
Primary 00011822741125
Unit of Use 00021292008116

Customer Contacts

Device Sizes

Type Value Unit Text
Needle Gauge 30 Gauge