gudid
Primary ID: 138334
ArgenTi 98.5x12 (UDI 138334)
Manufactured by ARGEN CORPORATION, THE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ArgenTi 98.5x12 - Primary ID 138334
Device Regulatory Overview
The ArgenTi 98.5x12 (Model/Catalog Number: 138334) 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
- 138334
- Product Code / EMDN
- EJH
- Device Name
- Base metal alloy
- Database Sync Date
- 2026-08-09 09:03:42
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of ArgenTi 98.5x12?
The registered manufacturer of record for ArgenTi 98.5x12 is ARGEN CORPORATION, THE.
What is the Primary UDI-DI identifier for ArgenTi 98.5x12?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 138334.
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
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