gudid
Primary ID: HS GENERAL PURPOSE
FLEXFORM LINE (UDI HS GENERAL PURPOSE)
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 FLEXFORM LINE - Primary ID HS GENERAL PURPOSE
Device Regulatory Overview
The FLEXFORM LINE (Model/Catalog Number: HS GENERAL PURPOSE) is a medical device manufactured by H.S. HOSPITAL SERVICE SPA. This product is indexed under FDA Product Code / Category Classification BSY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HS GENERAL PURPOSE
- Product Code / EMDN
- BSY
- Device Name
- HS GENERAL PURPOSE L 10FRX30CM
- 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 FLEXFORM LINE?
The registered manufacturer of record for FLEXFORM LINE is H.S. HOSPITAL SERVICE SPA.
What is the Primary UDI-DI identifier for FLEXFORM LINE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is HS GENERAL PURPOSE.
What classification code is assigned to this device?
This device is registered under product classification code BSY.
Similar Classification Devices (BSY)
Other Devices by H.S. HOSPITAL SERVICE SPA
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