eudamed_udi
Primary ID: 06945115402063
KAWA (UDI 06945115402063)
Manufactured by Weifang KAWA Medical Products Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KAWA - Primary ID 06945115402063
Device Regulatory Overview
The KAWA (Model/Catalog Number: 5ADMA004N) is a medical device manufactured by Weifang KAWA Medical Products Co., Ltd.. This product is indexed under FDA Product Code / Category Classification A03010199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 5ADMA004N
- Product Code / EMDN
- A03010199
- Device Name
- Sterile Infusion set for single use
- Database Sync Date
- 2026-08-09 17:00:09
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of KAWA?
The registered manufacturer of record for KAWA is Weifang KAWA Medical Products Co., Ltd..
What is the Primary UDI-DI identifier for KAWA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06945115402063.
What classification code is assigned to this device?
This device is registered under product classification code A03010199.
Similar Classification Devices (A03010199)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint