eudamed_udi
Primary ID: 08023279208016
CAPPELLINO FANTASIA - Fenicotteri - M (UDI 08023279208016)
Manufactured by GIMA SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CAPPELLINO FANTASIA - Fenicotteri - M - Primary ID 08023279208016
Device Regulatory Overview
The CAPPELLINO FANTASIA - Fenicotteri - M (Model/Catalog Number: 20801) is a medical device manufactured by GIMA SPA. This product is indexed under FDA Product Code / Category Classification T0207 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 20801
- Product Code / EMDN
- T0207
- Device Name
- CAPPELLINI RIUTILIZZABILI
- Database Sync Date
- 2026-08-09 16:44:51
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 CAPPELLINO FANTASIA - Fenicotteri - M?
The registered manufacturer of record for CAPPELLINO FANTASIA - Fenicotteri - M is GIMA SPA.
What is the Primary UDI-DI identifier for CAPPELLINO FANTASIA - Fenicotteri - M?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08023279208016.
What classification code is assigned to this device?
This device is registered under product classification code T0207.
Similar Classification Devices (T0207)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint