ProSeal CSTD Secondary Set with one way Valve (0.2 µm Filter) (UDI 18859299133598)
Manufactured by Epic International (Thailand) Co., Ltd.
Device Regulatory Overview
The ProSeal CSTD Secondary Set with one way Valve (0.2 µm Filter) (Model/Catalog Number: 423590) is a medical device manufactured by Epic International (Thailand) Co., Ltd.. This product is indexed under FDA Product Code / Category Classification A0399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 423590
- Product Code / EMDN
- A0399
- Device Name
- CSTD and Administration Devices
- Database Sync Date
- 2026-08-09 16:30:15
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 ProSeal CSTD Secondary Set with one way Valve (0.2 µm Filter)?
The registered manufacturer of record for ProSeal CSTD Secondary Set with one way Valve (0.2 µm Filter) is Epic International (Thailand) Co., Ltd..
What is the Primary UDI-DI identifier for ProSeal CSTD Secondary Set with one way Valve (0.2 µm Filter)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 18859299133598.
What classification code is assigned to this device?
This device is registered under product classification code A0399.
Similar Classification Devices (A0399)
Other Devices by Epic International (Thailand) Co., Ltd.
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