GUDIDData
eudamed_udi Primary ID: 14049538332668

nopa (UDI 14049538332668)

Manufactured by nopa instruments Medizintechnik GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for nopa - Primary ID 14049538332668

Device Regulatory Overview

The nopa (Model/Catalog Number: KP 378/12) is a medical device manufactured by nopa instruments Medizintechnik GmbH. This product is indexed under FDA Product Code / Category Classification L01040503 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
KP 378/12
Product Code / EMDN
L01040503
Device Name
Schere, Auge
Database Sync Date
2026-08-09 16:28:47

Full Regulatory Attributes

πŸ”’ 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 nopa?

The registered manufacturer of record for nopa is nopa instruments Medizintechnik GmbH.

What is the Primary UDI-DI identifier for nopa?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 14049538332668.

What classification code is assigned to this device?

This device is registered under product classification code L01040503.

Similar Classification Devices (L01040503)

Other Devices by nopa instruments Medizintechnik GmbH

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