FDA UDI In Commercial Distribution 🇺🇸 United States

Wondfo

DI: 00816862021905 · Model: W1-S3 · WONDFO USA CO., LTD.
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Wondfo
Primary DI
00816862021905
Version / Model
W1-S3
Company Name
WONDFO USA CO., LTD.
Labeler DUNS
849098897
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2020-02-20
Public Version
4
Public Version Date
2023-07-06
Public Version Status
Update
Public Device Record Key
a2cd3715-655e-4d95-83c4-1f4d3af51fb2

Device Description

1 Strip; hCG Serum/Urine Test Strip

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
LCX Kit, Test, Pregnancy, Hcg, Over The Counter
JHI Visual, Pregnancy Hcg, Prescription Use

GMDN Terms

Code Name
33819 Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical

Identifiers

Type ID
Package 00816862021929
Primary 00816862021905
Unit of Use 00816862021912

Customer Contacts

Phone
630-468-2199

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
4 – 30 Degrees Celsius