GUDIDData
eudamed_udi Primary ID: 06932825305388

ADEF (UDI 06932825305388)

Manufactured by Guangdong Transtek Medical Electronics Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ADEF - Primary ID 06932825305388

Device Regulatory Overview

The ADEF (Model/Catalog Number: AC2242-31) is a medical device manufactured by Guangdong Transtek Medical Electronics Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Z1203020302 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
AC2242-31
Product Code / EMDN
Z1203020302
Device Name
Cuff
Database Sync Date
2026-08-09 16:28:55

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 ADEF?

The registered manufacturer of record for ADEF is Guangdong Transtek Medical Electronics Co., Ltd..

What is the Primary UDI-DI identifier for ADEF?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06932825305388.

What classification code is assigned to this device?

This device is registered under product classification code Z1203020302.

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