FDA UDI In Commercial Distribution 🇺🇸 United States

Natalist Pregnancy Test

DI: 00860001730203 · Model: 82214 · Equinox Biotech Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Natalist Pregnancy Test
Primary DI
00860001730203
Version / Model
82214
Company Name
Equinox Biotech Co., Ltd.
Labeler DUNS
545868502
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-07-13
Public Version
4
Public Version Date
2023-07-06
Public Version Status
Update
Public Device Record Key
d540e75d-566c-4291-835e-6f7dfe06d279

Device Description

Natalist Pregnancy Test is intended for the qualitative determination of human chorionic gonadotropin (hCG) in the urine to aid in early detection of pregnancy. There are 3 6mm midstreams in one box.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
Yes
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
Primary 00860001730203

Customer Contacts

Storage Conditions

Type
Storage Environment Atmospheric Pressure
Temperature Range
35.6 – 86 Degrees Fahrenheit