gudid
Primary ID: SET A2 50 CAP
Set (UDI SET A2 50 CAP)
Manufactured by SDI LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Set - Primary ID SET A2 50 CAP
Device Regulatory Overview
The Set (Model/Catalog Number: SET A2 50 CAP) is a medical device manufactured by SDI LIMITED. This product is indexed under FDA Product Code / Category Classification EMA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SET A2 50 CAP
- Product Code / EMDN
- EMA
- Device Name
- Database Sync Date
- 2026-08-09 09:01:02
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 Set?
The registered manufacturer of record for Set is SDI LIMITED.
What is the Primary UDI-DI identifier for Set?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SET A2 50 CAP.
What classification code is assigned to this device?
This device is registered under product classification code EMA.
Similar Classification Devices (EMA)
Other Devices by SDI LIMITED
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