gudid
Primary ID: A01-SLB
MEMASA (UDI A01-SLB)
Manufactured by ShenZhen GoodlyMed Technology Co.,Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MEMASA - Primary ID A01-SLB
Device Regulatory Overview
The MEMASA (Model/Catalog Number: A01-SLB) is a medical device manufactured by ShenZhen GoodlyMed Technology Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification DXN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- A01-SLB
- Product Code / EMDN
- DXN
- Device Name
- Database Sync Date
- 2026-08-09 09:18:21
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of MEMASA?
The registered manufacturer of record for MEMASA is ShenZhen GoodlyMed Technology Co.,Ltd..
What is the Primary UDI-DI identifier for MEMASA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is A01-SLB.
What classification code is assigned to this device?
This device is registered under product classification code DXN.
Similar Classification Devices (DXN)
Other Devices by ShenZhen GoodlyMed Technology Co.,Ltd.
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