GUDIDData
eudamed_udi Primary ID: 04717237078448

PE Finger Splint, 4.9cm (UDI 04717237078448)

Manufactured by I-Ming Sanitary Materials Co.,Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PE Finger Splint, 4.9cm - Primary ID 04717237078448

Device Regulatory Overview

The PE Finger Splint, 4.9cm (Model/Catalog Number: OO-205) is a medical device manufactured by I-Ming Sanitary Materials Co.,Ltd. This product is indexed under FDA Product Code / Category Classification Y060603 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
OO-205
Product Code / EMDN
Y060603
Device Name
FINGERS ORTHOSES
Database Sync Date
2026-08-09 16:29:34

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 PE Finger Splint, 4.9cm?

The registered manufacturer of record for PE Finger Splint, 4.9cm is I-Ming Sanitary Materials Co.,Ltd.

What is the Primary UDI-DI identifier for PE Finger Splint, 4.9cm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04717237078448.

What classification code is assigned to this device?

This device is registered under product classification code Y060603.

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