FDA UDI In Commercial Distribution 🇺🇸 United States

Wondfo Pregnancy Test

DI: 00816862020342 · Model: W1-C · WONDFO USA CO., LTD.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
25

Basic Information

Brand Name
Wondfo Pregnancy Test
Primary DI
00816862020342
Version / Model
W1-C
Catalog Number
W1-C
Company Name
WONDFO USA CO., LTD.
Labeler DUNS
849098897
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2016-09-20
Public Version
5
Public Version Date
2023-07-06
Public Version Status
Update
Public Device Record Key
8d5cabdd-5910-46ef-ae6c-40bb990ec909

Device Description

1-Panel Cassette; hCG Pregnancy Test

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

GMDN Terms

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

Identifiers

Type ID
Package 10816862020349
Primary 00816862020342
Unit of Use 00816862029345

Customer Contacts

Phone
630-468-2199

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
4 – 30 Degrees Celsius