FDA UDI In Commercial Distribution 🇺🇸 United States

WELLlife™

DI: 00816862024722 · Model: WV01P0001-25 · WONDFO USA CO., LTD.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
25

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Basic Information

Brand Name
WELLlife™
Primary DI
00816862024722
Version / Model
WV01P0001-25
Company Name
WONDFO USA CO., LTD.
Labeler DUNS
849098897
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2024-12-20
Public Version
1
Public Version Date
2024-12-30
Public Version Status
New
Public Device Record Key
c0aec573-3d15-4c60-9efc-6033e6f6eecb

Device Description

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

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
Yes
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
QMN Covid-19 Multi-Analyte Antigen Device

GMDN Terms

Code Name
65454 SARS-CoV-2 antigen IVD, kit, rapid ICT, self-testing

Identifiers

Type ID
Package 10816862024729
Primary 00816862024722
Unit of Use 00816862024715

Customer Contacts

Phone
630-468-2199

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
4 – 30 Degrees Celsius