Multi-Patient Transfer Tube (UDI 06941944527960)
Manufactured by Shenzhen Maiwei Biotech Co., Ltd.
Device Regulatory Overview
The Multi-Patient Transfer Tube (Model/Catalog Number: D1L020M) is a medical device manufactured by Shenzhen Maiwei Biotech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification A03020102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- D1L020M
- Product Code / EMDN
- A03020102
- Device Name
- Multi-Patient Transfer Tube
- Database Sync Date
- 2026-08-09 16:28:58
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 Transfer Tube?
The registered manufacturer of record for Multi-Patient Transfer Tube is Shenzhen Maiwei Biotech Co., Ltd..
What is the Primary UDI-DI identifier for Multi-Patient Transfer Tube?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06941944527960.
What classification code is assigned to this device?
This device is registered under product classification code A03020102.
Similar Classification Devices (A03020102)
Other Devices by Shenzhen Maiwei Biotech Co., Ltd.
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