gudid
Primary ID: 128512
SLM PARTIAL POWDER(5 kg) (UDI 128512)
Manufactured by ARGEN CORPORATION, THE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SLM PARTIAL POWDER(5 kg) - Primary ID 128512
Device Regulatory Overview
The SLM PARTIAL POWDER(5 kg) (Model/Catalog Number: 128512) is a medical device manufactured by ARGEN CORPORATION, THE. This product is indexed under FDA Product Code / Category Classification EJH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 128512
- Product Code / EMDN
- EJH
- Device Name
- Base metal alloy
- Database Sync Date
- 2026-08-09 09:03:42
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 SLM PARTIAL POWDER(5 kg)?
The registered manufacturer of record for SLM PARTIAL POWDER(5 kg) is ARGEN CORPORATION, THE.
What is the Primary UDI-DI identifier for SLM PARTIAL POWDER(5 kg)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 128512.
What classification code is assigned to this device?
This device is registered under product classification code EJH.
Similar Classification Devices (EJH)
Other Devices by ARGEN CORPORATION, THE
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint