FDA UDI In Commercial Distribution 🇺🇸 United States

TRUEdraw

DI: 00050428645949 · Model: CVS TRUEdraw Lancing Device · TRIVIDIA HEALTH, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
TRUEdraw
Primary DI
00050428645949
Version / Model
CVS TRUEdraw Lancing Device
Catalog Number
S3007-01
Company Name
TRIVIDIA HEALTH, INC.
Labeler DUNS
151810868
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-12-31
Public Version
2
Public Version Date
2022-11-17
Public Version Status
Update
Public Device Record Key
6a102dd2-3ca6-4e85-a6d4-f756de6f2e9f

Device Description

CVS TRUEdraw Lancing Device

Device Characteristics

Single Use
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
QRL Multiple Use Blood Lancet For Single Patient Use Only

GMDN Terms

Code Name
37243 Manual blood lancing device, reusable

Identifiers

Type ID
Package 10050428645946
Primary 00050428645949

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K221072 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store at room temperature. Store without a lancet inserted.