Multi-Patient Syringe System (UDI 06945764435566)
Manufactured by Shenzhen Antmed Co., Ltd
Device Regulatory Overview
The Multi-Patient Syringe System (Model/Catalog Number: M110403) is a medical device manufactured by Shenzhen Antmed Co., Ltd. This product is indexed under FDA Product Code / Category Classification A020102010202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- M110403
- Product Code / EMDN
- A020102010202
- Device Name
- Multi-Patient Syringe System
- Database Sync Date
- 2026-08-09 16:48:57
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 Multi-Patient Syringe System?
The registered manufacturer of record for Multi-Patient Syringe System is Shenzhen Antmed Co., Ltd.
What is the Primary UDI-DI identifier for Multi-Patient Syringe System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06945764435566.
What classification code is assigned to this device?
This device is registered under product classification code A020102010202.
Similar Classification Devices (A020102010202)
Other Devices by Shenzhen Antmed Co., Ltd
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