eudamed_udi
Primary ID: 08011809998964
MAGLIA TUBOLARE NON STERILE (UDI 08011809998964)
Manufactured by Santex S.p.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MAGLIA TUBOLARE NON STERILE - Primary ID 08011809998964
Device Regulatory Overview
The MAGLIA TUBOLARE NON STERILE (Model/Catalog Number: MAG08S.) is a medical device manufactured by Santex S.p.A.. This product is indexed under FDA Product Code / Category Classification M03030201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MAG08S.
- Product Code / EMDN
- M03030201
- Device Name
- Maglia tubolare sottogesso non sterile
- Database Sync Date
- 2026-08-09 16:48:31
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 MAGLIA TUBOLARE NON STERILE?
The registered manufacturer of record for MAGLIA TUBOLARE NON STERILE is Santex S.p.A..
What is the Primary UDI-DI identifier for MAGLIA TUBOLARE NON STERILE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08011809998964.
What classification code is assigned to this device?
This device is registered under product classification code M03030201.
Similar Classification Devices (M03030201)
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