GARZE IN COTONE LAPAROTOMICHE STERILI (UDI 08011809021020)
Manufactured by Santex S.p.A.
Device Regulatory Overview
The GARZE IN COTONE LAPAROTOMICHE STERILI (Model/Catalog Number: FEF32020F4A0520) is a medical device manufactured by Santex S.p.A.. This product is indexed under FDA Product Code / Category Classification M0201030101,M0201030201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FEF32020F4A0520
- Product Code / EMDN
- M0201030101,M0201030201
- Device Name
- GARZE LAPAROTOMICHE STERILI
- Database Sync Date
- 2026-08-09 16:47:10
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 IN COTONE LAPAROTOMICHE STERILI?
The registered manufacturer of record for GARZE IN COTONE LAPAROTOMICHE STERILI is Santex S.p.A..
What is the Primary UDI-DI identifier for GARZE IN COTONE LAPAROTOMICHE STERILI?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08011809021020.
What classification code is assigned to this device?
This device is registered under product classification code M0201030101,M0201030201.
Similar Classification Devices (M0201030101,M0201030201)
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