gudid
Primary ID: AS3101004
SAINING (UDI AS3101004)
Manufactured by Zhejiang Saining Biotechnology Co., Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SAINING - Primary ID AS3101004
Device Regulatory Overview
The SAINING (Model/Catalog Number: AS3101004) is a medical device manufactured by Zhejiang Saining Biotechnology Co., Ltd. This product is indexed under FDA Product Code / Category Classification MXT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AS3101004
- Product Code / EMDN
- MXT
- Device Name
- Database Sync Date
- 2026-08-09 10:01:32
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 SAINING?
The registered manufacturer of record for SAINING is Zhejiang Saining Biotechnology Co., Ltd.
What is the Primary UDI-DI identifier for SAINING?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is AS3101004.
What classification code is assigned to this device?
This device is registered under product classification code MXT.
Similar Classification Devices (MXT)
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