eudamed_udi
Primary ID: D-0641053VB10000002VRAR
Gynolacta (UDI D-0641053VB10000002VRAR)
Manufactured by Vitabalans Oy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Gynolacta - Primary ID D-0641053VB10000002VRAR
Device Regulatory Overview
The Gynolacta (Model/Catalog Number: FI-CA01-2015-0884) is a medical device manufactured by Vitabalans Oy. This product is indexed under FDA Product Code / Category Classification U0803 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FI-CA01-2015-0884
- Product Code / EMDN
- U0803
- Device Name
- Vaginal tablet
- Database Sync Date
- 2026-08-09 16:46:59
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 Gynolacta?
The registered manufacturer of record for Gynolacta is Vitabalans Oy.
What is the Primary UDI-DI identifier for Gynolacta?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-0641053VB10000002VRAR.
What classification code is assigned to this device?
This device is registered under product classification code U0803.
Similar Classification Devices (U0803)
Other Devices by Vitabalans Oy
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint