FDA UDI In Commercial Distribution 🇺🇸 United States

WELLlife™

DI: 00816862027648 · Model: WFLUAB-OTC-25 · WONDFO USA CO., LTD.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
25

Basic Information

Brand Name
WELLlife™
Primary DI
00816862027648
Version / Model
WFLUAB-OTC-25
Company Name
WONDFO USA CO., LTD.
Labeler DUNS
849098897
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2025-09-05
Public Version
1
Public Version Date
2025-09-15
Public Version Status
New
Public Device Record Key
9c1032f1-28fe-4b26-9e9f-e18da0941bb0

Device Description

WELLlife™ COVID-19/Flu A&B Home Test Cassette, 25 Tests per Kitbox

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
No
Sterilization Prior Use
No

Product Codes

Code Name
SCA Multi-Analyte Respiratory Virus Antigen Detection Test

GMDN Terms

Code Name
66040 Multiple-genus respiratory virus antigen IVD, kit, rapid ICT, self-testing

Identifiers

Type ID
Package 10816862027645
Primary 00816862027648
Unit of Use 00816862027631

Customer Contacts

Phone
630-468-2199

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
4 – 30 Degrees Celsius