FDA UDI In Commercial Distribution 🇺🇸 United States

Preview

DI: 00816862021493 · Model: PRE-HCG-25S · WONDFO USA CO., LTD.
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
25

Basic Information

Brand Name
Preview
Primary DI
00816862021493
Version / Model
PRE-HCG-25S
Company Name
WONDFO USA CO., LTD.
Labeler DUNS
849098897
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2018-08-28
Public Version
4
Public Version Date
2023-07-06
Public Version Status
Update
Public Device Record Key
18ce2880-af54-492f-84ba-4a133006cb5b

Device Description

Preview hCG Pregnancy 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
JHI Visual, Pregnancy Hcg, Prescription Use
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 10816862021490
Primary 00816862021493
Unit of Use 00816862028492

Customer Contacts

Phone
8443372743

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
4 – 30 Degrees Celsius