FDA UDI In Commercial Distribution 🇺🇸 United States

Wondfo

DI: 00816862024302 · Model: W2-S50-CA · WONDFO USA CO., LTD.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

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Basic Information

Brand Name
Wondfo
Primary DI
00816862024302
Version / Model
W2-S50-CA
Company Name
WONDFO USA CO., LTD.
Labeler DUNS
849098897
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2024-12-24
Public Version
1
Public Version Date
2025-01-01
Public Version Status
New
Public Device Record Key
ef69bb14-cc91-4ff4-9779-ac7cef60044c

Device Description

50-Strip and 50 Plastic Urine Cups; LH-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 10816862024309
Primary 00816862024302
Unit of Use 00816862024319

Customer Contacts

Phone
630-468-2199

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
4 – 30 Degrees Celsius