GUDIDData
eudamed_udi Primary ID: 08059224160528

ESTR/CAPP. c/st. INSERITORE STRATEGY UDI (UDI 08059224160528)

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 ESTR/CAPP. c/st. INSERITORE STRATEGY UDI - Primary ID 08059224160528

Device Regulatory Overview

The ESTR/CAPP. c/st. INSERITORE STRATEGY UDI (Model/Catalog Number: 486ICS-US) 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
486ICS-US
Product Code / EMDN
Q010280
Device Name
Strumenti (Regola 1)
Database Sync Date
2026-08-09 16:29:06

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of ESTR/CAPP. c/st. INSERITORE STRATEGY UDI?

The registered manufacturer of record for ESTR/CAPP. c/st. INSERITORE STRATEGY UDI is Rhein 83 S.r.l..

What is the Primary UDI-DI identifier for ESTR/CAPP. c/st. INSERITORE STRATEGY UDI?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08059224160528.

What classification code is assigned to this device?

This device is registered under product classification code Q010280.

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