Multi-Respiratory Antigen Test (Swab) (UDI D-SWx5-RTC(PLUS)DS)
Manufactured by Aceso Laboratories, Inc.
Device Regulatory Overview
The Multi-Respiratory Antigen Test (Swab) (Model/Catalog Number: SWx5-RTC(PLUS)) is a medical device manufactured by Aceso Laboratories, Inc.. This product is indexed under FDA Product Code / Category Classification W0105070399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SWx5-RTC(PLUS)
- Product Code / EMDN
- W0105070399
- Device Name
- Multi-Respiratory Antigen Test (Swab)
- Database Sync Date
- 2026-08-09 16:30:25
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-Respiratory Antigen Test (Swab)?
The registered manufacturer of record for Multi-Respiratory Antigen Test (Swab) is Aceso Laboratories, Inc..
What is the Primary UDI-DI identifier for Multi-Respiratory Antigen Test (Swab)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-SWx5-RTC(PLUS)DS.
What classification code is assigned to this device?
This device is registered under product classification code W0105070399.
Similar Classification Devices (W0105070399)
Other Devices by Aceso Laboratories, Inc.
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