gudid
Primary ID: 7WFP51
N/A (UDI 7WFP51)
Manufactured by GALEMED CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for N/A - Primary ID 7WFP51
Device Regulatory Overview
The N/A (Model/Catalog Number: 7WFP51) is a medical device manufactured by GALEMED CORPORATION. This product is indexed under FDA Product Code / Category Classification BYH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7WFP51
- Product Code / EMDN
- BYH
- Device Name
- CS Water Trap Kit, L Type, 10M
- Database Sync Date
- 2026-08-09 09:15:32
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of N/A?
The registered manufacturer of record for N/A is GALEMED CORPORATION.
What is the Primary UDI-DI identifier for N/A?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 7WFP51.
What classification code is assigned to this device?
This device is registered under product classification code BYH.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint