eudamed_udi Primary ID: G520MD61030

Z Bend Plier Reg (UDI G520MD61030)

Manufactured by Medspo

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Z Bend Plier Reg (Model/Catalog Number: MD6103) is a medical device manufactured by Medspo. This product is indexed under FDA Product Code / Category Classification L150702 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: MD6103
Product Code / EMDN: L150702
Device Name: Z Bend Plier Reg
Database Sync Date: 2026-08-09 17:02:30

Full Regulatory Attributes

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{
    "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 Z Bend Plier Reg?

The registered manufacturer of record for Z Bend Plier Reg is Medspo.

What is the Primary UDI-DI identifier for Z Bend Plier Reg?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G520MD61030.

What classification code is assigned to this device?

This device is registered under product classification code L150702.

Similar Classification Devices (L150702)

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