gudid
Primary ID: 00022600900542
First Response Ovulation Test (UDI 00022600900542)
Manufactured by CHURCH & DWIGHT CO., INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for First Response Ovulation Test - Primary ID 00022600900542
Device Regulatory Overview
The First Response Ovulation Test (Model/Catalog Number: 00022600900542) is a medical device manufactured by CHURCH & DWIGHT CO., INC.. This product is indexed under FDA Product Code / Category Classification CEP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 00022600900542
- Product Code / EMDN
- CEP
- Device Name
- Database Sync Date
- 2026-08-09 09:00:33
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of First Response Ovulation Test?
The registered manufacturer of record for First Response Ovulation Test is CHURCH & DWIGHT CO., INC..
What is the Primary UDI-DI identifier for First Response Ovulation Test?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00022600900542.
What classification code is assigned to this device?
This device is registered under product classification code CEP.
Similar Classification Devices (CEP)
Other Devices by CHURCH & DWIGHT CO., INC.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint