FDA UDI In Commercial Distribution 🇺🇸 United States

First Response Early Result Pregnancy Test

DI: 00022600020141 · Model: 00022600020141 · CHURCH & DWIGHT CO., INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
First Response Early Result Pregnancy Test
Primary DI
00022600020141
Version / Model
00022600020141
Company Name
CHURCH & DWIGHT CO., INC.
Labeler DUNS
001211952
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-02-25
Public Version
2
Public Version Date
2023-07-06
Public Version Status
Update
Public Device Record Key
95716bf9-91a0-45b5-855a-7aa352c504e3

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
Yes
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 00022600020141

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K123436 000