eudamed_udi
Primary ID: 00810049431471
Theratogs (UDI 00810049431471)
Manufactured by Theratogs Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Theratogs - Primary ID 00810049431471
Device Regulatory Overview
The Theratogs (Model/Catalog Number: GCSS23) is a medical device manufactured by Theratogs Inc. This product is indexed under FDA Product Code / Category Classification Y060309 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- GCSS23
- Product Code / EMDN
- Y060309
- Device Name
- Theratogs Clinical Starter System
- Database Sync Date
- 2026-08-09 16:29:01
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 Theratogs?
The registered manufacturer of record for Theratogs is Theratogs Inc.
What is the Primary UDI-DI identifier for Theratogs?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00810049431471.
What classification code is assigned to this device?
This device is registered under product classification code Y060309.
Similar Classification Devices (Y060309)
Other Devices by Theratogs Inc
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint