eudamed_udi
Primary ID: 06954414798876
Getein (UDI 06954414798876)
Manufactured by Getein Biotech, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Getein - Primary ID 06954414798876
Device Regulatory Overview
The Getein (Model/Catalog Number: /) is a medical device manufactured by Getein Biotech, Inc.. This product is indexed under FDA Product Code / Category Classification W0102060202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- /
- Product Code / EMDN
- W0102060202
- Device Name
- MAGICL Angiotensin I (CLIA)
- Database Sync Date
- 2026-08-09 16:51:25
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 Getein?
The registered manufacturer of record for Getein is Getein Biotech, Inc..
What is the Primary UDI-DI identifier for Getein?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06954414798876.
What classification code is assigned to this device?
This device is registered under product classification code W0102060202.
Similar Classification Devices (W0102060202)
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