gudid
Primary ID: A.4019
Anoscope (UDI A.4019)
Manufactured by SAPI MED SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Anoscope - Primary ID A.4019
Device Regulatory Overview
The Anoscope (Model/Catalog Number: A.4019) is a medical device manufactured by SAPI MED SPA. This product is indexed under FDA Product Code / Category Classification FER within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- A.4019
- Product Code / EMDN
- FER
- Device Name
- Self-Light Diagnostic Proctoscope
- Database Sync Date
- 2026-08-09 09:04:39
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 Anoscope?
The registered manufacturer of record for Anoscope is SAPI MED SPA.
What is the Primary UDI-DI identifier for Anoscope?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is A.4019.
What classification code is assigned to this device?
This device is registered under product classification code FER.
Similar Classification Devices (FER)
Other Devices by SAPI MED SPA
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