gudid
Primary ID: RES037
Water Trap (UDI RES037)
Manufactured by SUNSET HEALTHCARE SOLUTIONS, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Water Trap - Primary ID RES037
Device Regulatory Overview
The Water Trap (Model/Catalog Number: RES037) is a medical device manufactured by SUNSET HEALTHCARE SOLUTIONS, INC.. This product is indexed under FDA Product Code / Category Classification BYH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RES037
- Product Code / EMDN
- BYH
- Device Name
- Water Trap (1/pack)
- Database Sync Date
- 2026-08-09 09:48:14
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 Water Trap?
The registered manufacturer of record for Water Trap is SUNSET HEALTHCARE SOLUTIONS, INC..
What is the Primary UDI-DI identifier for Water Trap?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RES037.
What classification code is assigned to this device?
This device is registered under product classification code BYH.
Similar Classification Devices (BYH)
Other Devices by SUNSET HEALTHCARE SOLUTIONS, INC.
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