GUDIDData
eudamed_udi Primary ID: 06970010880616

Unspecified Brand (UDI 06970010880616)

Manufactured by SHANGHAI KOHDEN MEDICAL ELECTRONIC INSTRUMENT CORP.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 06970010880616

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: NA) is a medical device manufactured by SHANGHAI KOHDEN MEDICAL ELECTRONIC INSTRUMENT CORP.. This product is indexed under FDA Product Code / Category Classification Z1203020280 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
NA
Product Code / EMDN
Z1203020280
Device Name
JP-751P
Database Sync Date
2026-08-09 16:29:29

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 Unspecified Brand?

The registered manufacturer of record for Unspecified Brand is SHANGHAI KOHDEN MEDICAL ELECTRONIC INSTRUMENT CORP..

What is the Primary UDI-DI identifier for Unspecified Brand?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06970010880616.

What classification code is assigned to this device?

This device is registered under product classification code Z1203020280.

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