eudamed_udi
Primary ID: 06923980110368
Low Flow Manifold (UDI 06923980110368)
Manufactured by GaleMed (Xiamen) Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Low Flow Manifold - Primary ID 06923980110368
Device Regulatory Overview
The Low Flow Manifold (Model/Catalog Number: XAI0001) is a medical device manufactured by GaleMed (Xiamen) Co., Ltd.. This product is indexed under FDA Product Code / Category Classification R028001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- XAI0001
- Product Code / EMDN
- R028001
- Device Name
- Disposable Valve & Manifold
- Database Sync Date
- 2026-08-09 16:50:17
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 Low Flow Manifold?
The registered manufacturer of record for Low Flow Manifold is GaleMed (Xiamen) Co., Ltd..
What is the Primary UDI-DI identifier for Low Flow Manifold?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06923980110368.
What classification code is assigned to this device?
This device is registered under product classification code R028001.
Similar Classification Devices (R028001)
Other Devices by GaleMed (Xiamen) Co., Ltd.
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