FDA UDI In Commercial Distribution 🇺🇸 United States

Shinetell Digital Pregnancy Test

DI: 06936983167130 · Model: 1 · Hangzhou AllTest Biotech Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
3

Basic Information

Brand Name
Shinetell Digital Pregnancy Test
Primary DI
06936983167130
Version / Model
1
Catalog Number
FHC-AE103H
Company Name
Hangzhou AllTest Biotech Co., Ltd.
Labeler DUNS
543254717
Distribution Status
In Commercial Distribution
Device Count in Pkg
3
Record Status
Published
Publish Date
2026-04-15
Public Version
1
Public Version Date
2026-04-23
Public Version Status
New
Public Device Record Key
719efee3-7663-4a62-878c-5baf3a05ef0f

Device Description

3T, FDA OTC

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Unit of Use 86936983167136
Primary 06936983167130