GUDIDData
eudamed_udi Primary ID: 04033789004156

Non-conductive tips T 200µL (UDI 04033789004156)

Manufactured by Ritter GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Non-conductive tips T 200µL - Primary ID 04033789004156

Device Regulatory Overview

The Non-conductive tips T 200µL (Model/Catalog Number: 49102-0006) is a medical device manufactured by Ritter GmbH. This product is indexed under FDA Product Code / Category Classification W0503020202 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
49102-0006
Product Code / EMDN
W0503020202
Device Name
Robotic tips
Database Sync Date
2026-08-09 16:44:54

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 Non-conductive tips T 200µL?

The registered manufacturer of record for Non-conductive tips T 200µL is Ritter GmbH.

What is the Primary UDI-DI identifier for Non-conductive tips T 200µL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04033789004156.

What classification code is assigned to this device?

This device is registered under product classification code W0503020202.

Programmatic Export

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

JSON API Endpoint