GUDIDData
Bulk Audit Tool API Access
eudamed_udi Primary ID: 08059224119458

PLUS CAPS INSERTION TOOL (UDI 08059224119458)

Manufactured by Rhein 83 S.r.l.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PLUS CAPS INSERTION TOOL - Primary ID 08059224119458

Device Regulatory Overview

The PLUS CAPS INSERTION TOOL (Model/Catalog Number: 083ICP) is a medical device manufactured by Rhein 83 S.r.l.. This product is indexed under FDA Product Code / Category Classification Q010280 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
083ICP
Product Code / EMDN
Q010280
Device Name
Strumenti (Regola 1)
Database Sync Date
2026-08-09 16:28:45

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 PLUS CAPS INSERTION TOOL?

The registered manufacturer of record for PLUS CAPS INSERTION TOOL is Rhein 83 S.r.l..

What is the Primary UDI-DI identifier for PLUS CAPS INSERTION TOOL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08059224119458.

What classification code is assigned to this device?

This device is registered under product classification code Q010280.

Similar Classification Devices (Q010280)

Other Devices by Rhein 83 S.r.l.

Programmatic Export

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

JSON API Endpoint