GUDIDData
eudamed_udi Primary ID: 06945632020894

XINLI (UDI 06945632020894)

Manufactured by Changzhou Tongda Medical Appliance Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for XINLI - Primary ID 06945632020894

Device Regulatory Overview

The XINLI (Model/Catalog Number: TD-TSG-B-0.36mm) is a medical device manufactured by Changzhou Tongda Medical Appliance Co., Ltd.. This product is indexed under FDA Product Code / Category Classification A03010102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
TD-TSG-B-0.36mm
Product Code / EMDN
A03010102
Device Name
Disposable Transfusion Sets (with Needle)
Database Sync Date
2026-08-09 16:29:33

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 XINLI?

The registered manufacturer of record for XINLI is Changzhou Tongda Medical Appliance Co., Ltd..

What is the Primary UDI-DI identifier for XINLI?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06945632020894.

What classification code is assigned to this device?

This device is registered under product classification code A03010102.

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