GUDIDData
gudid Primary ID: 10125L

Collin (UDI 10125L)

Manufactured by NETWORK MEDICAL PRODUCTS LIMITED

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Collin - Primary ID 10125L

Device Regulatory Overview

The Collin (Model/Catalog Number: 10125L) is a medical device manufactured by NETWORK MEDICAL PRODUCTS LIMITED. This product is indexed under FDA Product Code / Category Classification LYA within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
10125L
Product Code / EMDN
LYA
Device Name
Collin Anatomical Slimpack Layered 8.0cm - Carton
Database Sync Date
2026-08-09 09:08:11

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 Collin?

The registered manufacturer of record for Collin is NETWORK MEDICAL PRODUCTS LIMITED.

What is the Primary UDI-DI identifier for Collin?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10125L.

What classification code is assigned to this device?

This device is registered under product classification code LYA.

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