gudid
Primary ID: ACD-200B
SIMEOX 200 (UDI ACD-200B)
Manufactured by PHYSIO-ASSIST
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SIMEOX 200 - Primary ID ACD-200B
Device Regulatory Overview
The SIMEOX 200 (Model/Catalog Number: ACD-200B) is a medical device manufactured by PHYSIO-ASSIST. This product is indexed under FDA Product Code / Category Classification SDT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ACD-200B
- Product Code / EMDN
- SDT
- Device Name
- Simeox 200 airway clearance device with installed battery
- Database Sync Date
- 2026-08-09 09:52:17
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 SIMEOX 200?
The registered manufacturer of record for SIMEOX 200 is PHYSIO-ASSIST.
What is the Primary UDI-DI identifier for SIMEOX 200?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ACD-200B.
What classification code is assigned to this device?
This device is registered under product classification code SDT.
Similar Classification Devices (SDT)
Other Devices by PHYSIO-ASSIST
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