FDA UDI In Commercial Distribution 🇺🇸 United States

Wondfo

DI: 00816862022933 · Model: W2-S-SQ-20BX · WONDFO USA CO., LTD.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
20

Basic Information

Brand Name
Wondfo
Primary DI
00816862022933
Version / Model
W2-S-SQ-20BX
Catalog Number
W2-S-SQ-20BX
Company Name
WONDFO USA CO., LTD.
Labeler DUNS
849098897
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2021-08-20
Public Version
2
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
98643954-dc3c-4a39-8ec7-169dd5b16a34

Device Description

1-Strip; LH Semi Quantitative Ovulation Test

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
NGE Test, Luteinizing Hormone (Lh), Over The Counter

GMDN Terms

Code Name
54255 Luteinizing hormone (LH) IVD, kit, rapid ICT, clinical

Identifiers

Type ID
Package 10816862022930
Primary 00816862022933
Unit of Use 00816862022940

Customer Contacts

Phone
630-468-2199

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
4 – 30 Degrees Celsius