eudamed_udi
Primary ID: 04255908500435
M59 48◻20 143 C24 (UDI 04255908500435)
Manufactured by Alpha Collection
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for M59 48◻20 143 C24 - Primary ID 04255908500435
Device Regulatory Overview
The M59 48◻20 143 C24 (Model/Catalog Number: www.alphacollection.com) is a medical device manufactured by Alpha Collection. This product is indexed under FDA Product Code / Category Classification Q02100202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- www.alphacollection.com
- Product Code / EMDN
- Q02100202
- Device Name
- fullrim plastic spectacle frames
- Database Sync Date
- 2026-08-09 16:30:09
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 M59 48◻20 143 C24?
The registered manufacturer of record for M59 48◻20 143 C24 is Alpha Collection.
What is the Primary UDI-DI identifier for M59 48◻20 143 C24?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04255908500435.
What classification code is assigned to this device?
This device is registered under product classification code Q02100202.
Similar Classification Devices (Q02100202)
Other Devices by Alpha Collection
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