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gudid Primary ID: WT-96131

WATEER TRAP(SCREW CAP) (UDI WT-96131)

Manufactured by BESMED HEALTH BUSINESS CORP.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for WATEER TRAP(SCREW CAP) - Primary ID WT-96131

Device Regulatory Overview

The WATEER TRAP(SCREW CAP) (Model/Catalog Number: WT-96131) is a medical device manufactured by BESMED HEALTH BUSINESS CORP.. This product is indexed under FDA Product Code / Category Classification BYX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
WT-96131
Product Code / EMDN
BYX
Device Name
WATEER TRAP(SCREW CAP)
Database Sync Date
2026-08-09 09:15:29

Full Regulatory Attributes

🔒 Token Gated 
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of WATEER TRAP(SCREW CAP)?

The registered manufacturer of record for WATEER TRAP(SCREW CAP) is BESMED HEALTH BUSINESS CORP..

What is the Primary UDI-DI identifier for WATEER TRAP(SCREW CAP)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is WT-96131.

What classification code is assigned to this device?

This device is registered under product classification code BYX.

Similar Classification Devices (BYX)

Other Devices by BESMED HEALTH BUSINESS CORP.

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