Set PP (UDI SET PP MIXING TIPS (REGULAR))

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Set PP (Model/Catalog Number: SET PP MIXING TIPS (REGULAR)) is a medical device manufactured by SDI LIMITED. This product is indexed under FDA Product Code / Category Classification EMA within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: SET PP MIXING TIPS (REGULAR)
Product Code / EMDN: EMA
Device Name
Database Sync Date: 2026-08-09 09:01:02

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 Set PP?

The registered manufacturer of record for Set PP is SDI LIMITED.

What is the Primary UDI-DI identifier for Set PP?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SET PP MIXING TIPS (REGULAR).

What classification code is assigned to this device?

This device is registered under product classification code EMA.

Similar Classification Devices (EMA)

Other Devices by SDI LIMITED

Programmatic Export

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

JSON API Endpoint