ToxiSeal Vial Adaptor (DMA Compatible) for 20 mm Vial Concave (UDI 58859299130434)
Manufactured by Epic International (Thailand) Co., Ltd.
Device Regulatory Overview
The ToxiSeal Vial Adaptor (DMA Compatible) for 20 mm Vial Concave (Model/Catalog Number: 420435) is a medical device manufactured by Epic International (Thailand) Co., Ltd.. This product is indexed under FDA Product Code / Category Classification A0704 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 420435
- Product Code / EMDN
- A0704
- Device Name
- CSTD and Administration Devices
- Database Sync Date
- 2026-08-09 16:28:46
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 ToxiSeal Vial Adaptor (DMA Compatible) for 20 mm Vial Concave?
The registered manufacturer of record for ToxiSeal Vial Adaptor (DMA Compatible) for 20 mm Vial Concave is Epic International (Thailand) Co., Ltd..
What is the Primary UDI-DI identifier for ToxiSeal Vial Adaptor (DMA Compatible) for 20 mm Vial Concave?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 58859299130434.
What classification code is assigned to this device?
This device is registered under product classification code A0704.
Similar Classification Devices (A0704)
Other Devices by Epic International (Thailand) Co., Ltd.
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- → SMARTeZ Plus-General Infusion 250-250-60m
- → SMARTeZ RS-General Infusion 250-175-1.5h with Hanger Cap
- → SMARTeZ Plus-PainBloc-Variable Flow with Bolus Volume 270ml flow 2-14ml/h Bolus 2ml Refill 30 min Single Hanger Cap
Programmatic Export
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JSON API Endpoint