gudid
Primary ID: AMICA-PROBE
HS AMICA (UDI AMICA-PROBE)
Manufactured by H.S. HOSPITAL SERVICE SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HS AMICA - Primary ID AMICA-PROBE
Device Regulatory Overview
The HS AMICA (Model/Catalog Number: AMICA-PROBE) is a medical device manufactured by H.S. HOSPITAL SERVICE SPA. This product is indexed under FDA Product Code / Category Classification GEI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AMICA-PROBE
- Product Code / EMDN
- GEI
- Device Name
- AMICA-PROBE 18GX100MM
- Database Sync Date
- 2026-08-09 09:05:05
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 HS AMICA?
The registered manufacturer of record for HS AMICA is H.S. HOSPITAL SERVICE SPA.
What is the Primary UDI-DI identifier for HS AMICA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is AMICA-PROBE.
What classification code is assigned to this device?
This device is registered under product classification code GEI.
Similar Classification Devices (GEI)
Other Devices by H.S. HOSPITAL SERVICE SPA
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