FDA UDI In Commercial Distribution 🇺🇸 United States

THERA Plus

DI: 00049696186773 · Model: 64431942AA · FOURSTAR GROUP INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
THERA Plus
Primary DI
00049696186773
Version / Model
64431942AA
Company Name
FOURSTAR GROUP INC.
Labeler DUNS
656091279
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-27
Public Version
1
Public Version Date
2023-11-06
Public Version Status
New
Public Device Record Key
b68d1037-6ca4-4490-a645-5d1c1a4d170a

Device Description

Lancets 200CT

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
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
Yes
Sterilization Methods
Radiation Sterilization

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
Primary 00049696186773

Premarket Submissions

Submission Number Supplement Number
K222472 000