GUDIDData
eudamed_udi Primary ID: D-509939041496775

FLEMING MEDICAL (UDI D-509939041496775)

Manufactured by Radiant Innovation Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FLEMING MEDICAL - Primary ID D-509939041496775

Device Regulatory Overview

The FLEMING MEDICAL (Model/Catalog Number: MD1882) is a medical device manufactured by Radiant Innovation Inc.. This product is indexed under FDA Product Code / Category Classification V0301010202 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
MD1882
Product Code / EMDN
V0301010202
Device Name
TH809S
Database Sync Date
2026-08-09 17:33:12

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 FLEMING MEDICAL?

The registered manufacturer of record for FLEMING MEDICAL is Radiant Innovation Inc..

What is the Primary UDI-DI identifier for FLEMING MEDICAL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-509939041496775.

What classification code is assigned to this device?

This device is registered under product classification code V0301010202.

Programmatic Export

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

JSON API Endpoint