GUDIDData
gudid Primary ID: 1911000

WATER TRAP, SELF SEALING MEDIUM VOLUME (UDI 1911000)

Manufactured by Intersurgical Incorporated

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for WATER TRAP, SELF SEALING MEDIUM VOLUME - Primary ID 1911000

Device Regulatory Overview

The WATER TRAP, SELF SEALING MEDIUM VOLUME (Model/Catalog Number: 1911000) is a medical device manufactured by Intersurgical Incorporated. This product is indexed under FDA Product Code / Category Classification BYH within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
1911000
Product Code / EMDN
BYH
Device Name
WATER TRAP, SELF SEALING MEDIUM VOLUME
Database Sync Date
2026-08-09 09:45:58

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 WATER TRAP, SELF SEALING MEDIUM VOLUME?

The registered manufacturer of record for WATER TRAP, SELF SEALING MEDIUM VOLUME is Intersurgical Incorporated.

What is the Primary UDI-DI identifier for WATER TRAP, SELF SEALING MEDIUM VOLUME?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1911000.

What classification code is assigned to this device?

This device is registered under product classification code BYH.

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