gudid
Primary ID: C235
C235 (UDI C235)
Manufactured by EKOM spol. s r.o.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for C235 - Primary ID C235
Device Regulatory Overview
The C235 (Model/Catalog Number: C235) is a medical device manufactured by EKOM spol. s r.o.. This product is indexed under FDA Product Code / Category Classification BTI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- C235
- Product Code / EMDN
- BTI
- Device Name
- Database Sync Date
- 2026-08-09 09:41:10
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 C235?
The registered manufacturer of record for C235 is EKOM spol. s r.o..
What is the Primary UDI-DI identifier for C235?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is C235.
What classification code is assigned to this device?
This device is registered under product classification code BTI.
Similar Classification Devices (BTI)
Other Devices by EKOM spol. s r.o.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint