gudid Primary ID: P02-WB902-10

Medegen Medical Products, LLC (UDI P02-WB902-10)

Manufactured by MEDEGEN MEDICAL PRODUCTS, LLC

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Medegen Medical Products, LLC (Model/Catalog Number: P02-WB902-10) is a medical device manufactured by MEDEGEN MEDICAL PRODUCTS, LLC. This product is indexed under FDA Product Code / Category Classification FMH within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: P02-WB902-10
Product Code / EMDN: FMH
Device Name: Spec Cont 90ml Wide St 400/cs 20/plt
Database Sync Date: 2026-08-09 09:04:15

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 Medegen Medical Products, LLC?

The registered manufacturer of record for Medegen Medical Products, LLC is MEDEGEN MEDICAL PRODUCTS, LLC.

What is the Primary UDI-DI identifier for Medegen Medical Products, LLC?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is P02-WB902-10.

What classification code is assigned to this device?

This device is registered under product classification code FMH.

Similar Classification Devices (FMH)

Other Devices by MEDEGEN MEDICAL PRODUCTS, LLC

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint