gudid
Primary ID: A.5660
Haemorrhoid ligator (UDI A.5660)
Manufactured by SAPI MED SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Haemorrhoid ligator - Primary ID A.5660
Device Regulatory Overview
The Haemorrhoid ligator (Model/Catalog Number: A.5660) is a medical device manufactured by SAPI MED SPA. This product is indexed under FDA Product Code / Category Classification FHN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- A.5660
- Product Code / EMDN
- FHN
- Device Name
- LEM haemorrhoid banding ligator use with forceps
- 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 Haemorrhoid ligator?
The registered manufacturer of record for Haemorrhoid ligator is SAPI MED SPA.
What is the Primary UDI-DI identifier for Haemorrhoid ligator?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is A.5660.
What classification code is assigned to this device?
This device is registered under product classification code FHN.
Similar Classification Devices (FHN)
Other Devices by SAPI MED SPA
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