gudid
Primary ID: ALLIVE3
ELEXIR 2.0 (UDI ALLIVE3)
Manufactured by Nu Eyne Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ELEXIR 2.0 - Primary ID ALLIVE3
Device Regulatory Overview
The ELEXIR 2.0 (Model/Catalog Number: ALLIVE3) is a medical device manufactured by Nu Eyne Co., Ltd.. This product is indexed under FDA Product Code / Category Classification PCC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ALLIVE3
- Product Code / EMDN
- PCC
- Device Name
- Database Sync Date
- 2026-08-09 09:13:02
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 ELEXIR 2.0?
The registered manufacturer of record for ELEXIR 2.0 is Nu Eyne Co., Ltd..
What is the Primary UDI-DI identifier for ELEXIR 2.0?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ALLIVE3.
What classification code is assigned to this device?
This device is registered under product classification code PCC.
Similar Classification Devices (PCC)
Other Devices by Nu Eyne Co., Ltd.
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