gudid
Primary ID: SA 201 (Spanish)
Entomed By Auditdata (UDI SA 201 (Spanish))
Manufactured by Auditdata A/S
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Entomed By Auditdata - Primary ID SA 201 (Spanish)
Device Regulatory Overview
The Entomed By Auditdata (Model/Catalog Number: SA 201 (Spanish)) is a medical device manufactured by Auditdata A/S. This product is indexed under FDA Product Code / Category Classification EWO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SA 201 (Spanish)
- Product Code / EMDN
- EWO
- Device Name
- Database Sync Date
- 2026-08-09 09:12:44
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 Entomed By Auditdata?
The registered manufacturer of record for Entomed By Auditdata is Auditdata A/S.
What is the Primary UDI-DI identifier for Entomed By Auditdata?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SA 201 (Spanish).
What classification code is assigned to this device?
This device is registered under product classification code EWO.
Similar Classification Devices (EWO)
Other Devices by Auditdata A/S
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