eudamed_udi
Primary ID: 08011809999121
OVATTA ORTOPEDICA SOTTOGESSO NON STERILE (UDI 08011809999121)
Manufactured by Santex S.p.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for OVATTA ORTOPEDICA SOTTOGESSO NON STERILE - Primary ID 08011809999121
Device Regulatory Overview
The OVATTA ORTOPEDICA SOTTOGESSO NON STERILE (Model/Catalog Number: VSB015N) is a medical device manufactured by Santex S.p.A.. This product is indexed under FDA Product Code / Category Classification M01020202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- VSB015N
- Product Code / EMDN
- M01020202
- Device Name
- Ovatta ortopedica sottogesso non sterile
- Database Sync Date
- 2026-08-09 16:30:37
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 OVATTA ORTOPEDICA SOTTOGESSO NON STERILE?
The registered manufacturer of record for OVATTA ORTOPEDICA SOTTOGESSO NON STERILE is Santex S.p.A..
What is the Primary UDI-DI identifier for OVATTA ORTOPEDICA SOTTOGESSO NON STERILE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08011809999121.
What classification code is assigned to this device?
This device is registered under product classification code M01020202.
Similar Classification Devices (M01020202)
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