eudamed_udi
Primary ID: 08809327356188
ClearCap Distal Attachment (UDI 08809327356188)
Manufactured by FINEMEDIX CO., LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ClearCap Distal Attachment - Primary ID 08809327356188
Device Regulatory Overview
The ClearCap Distal Attachment (Model/Catalog Number: FM-CC06) is a medical device manufactured by FINEMEDIX CO., LTD.. This product is indexed under FDA Product Code / Category Classification K0180 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FM-CC06
- Product Code / EMDN
- K0180
- Device Name
- Single-Use Endoscopic Distal Attachment Cap
- Database Sync Date
- 2026-08-09 16:28:56
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 ClearCap Distal Attachment?
The registered manufacturer of record for ClearCap Distal Attachment is FINEMEDIX CO., LTD..
What is the Primary UDI-DI identifier for ClearCap Distal Attachment?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08809327356188.
What classification code is assigned to this device?
This device is registered under product classification code K0180.
Similar Classification Devices (K0180)
Other Devices by FINEMEDIX CO., LTD.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint