GARZE LAPAROTOMICHE NON STERILI (UDI 08011809021310)
Manufactured by Santex S.p.A.
Device Regulatory Overview
The GARZE LAPAROTOMICHE NON STERILI (Model/Catalog Number: FR3D4040X4INABL) is a medical device manufactured by Santex S.p.A.. This product is indexed under FDA Product Code / Category Classification M0201030102,M0201030202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FR3D4040X4INABL
- Product Code / EMDN
- M0201030102,M0201030202
- Device Name
- FALDELLE NON STERILI/STERILIZZABILI
- Database Sync Date
- 2026-08-09 16:49:42
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 GARZE LAPAROTOMICHE NON STERILI?
The registered manufacturer of record for GARZE LAPAROTOMICHE NON STERILI is Santex S.p.A..
What is the Primary UDI-DI identifier for GARZE LAPAROTOMICHE NON STERILI?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08011809021310.
What classification code is assigned to this device?
This device is registered under product classification code M0201030102,M0201030202.
Similar Classification Devices (M0201030102,M0201030202)
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