GUDIDData
eudamed_udi Primary ID: 08051277606565

GUANCIALE ORIGINAL DELUXE 7 CE OBI (UDI 08051277606565)

Manufactured by TECHNOGEL ITALIA SRL

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GUANCIALE ORIGINAL DELUXE 7 CE OBI - Primary ID 08051277606565

Device Regulatory Overview

The GUANCIALE ORIGINAL DELUXE 7 CE OBI (Model/Catalog Number: TG-PIL1D07OB) is a medical device manufactured by TECHNOGEL ITALIA SRL. This product is indexed under FDA Product Code / Category Classification V080399 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
TG-PIL1D07OB
Product Code / EMDN
V080399
Device Name
ORIGINAL DELUXE
Database Sync Date
2026-08-09 16:28:47

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 GUANCIALE ORIGINAL DELUXE 7 CE OBI?

The registered manufacturer of record for GUANCIALE ORIGINAL DELUXE 7 CE OBI is TECHNOGEL ITALIA SRL.

What is the Primary UDI-DI identifier for GUANCIALE ORIGINAL DELUXE 7 CE OBI?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08051277606565.

What classification code is assigned to this device?

This device is registered under product classification code V080399.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint