eudamed_udi
Primary ID: 08011809022553
TAMPONI DI GARZA NON STERILI (UDI 08011809022553)
Manufactured by Santex S.p.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TAMPONI DI GARZA NON STERILI - Primary ID 08011809022553
Device Regulatory Overview
The TAMPONI DI GARZA NON STERILI (Model/Catalog Number: ZTRS30FI) is a medical device manufactured by Santex S.p.A.. This product is indexed under FDA Product Code / Category Classification M0201050102,M0201050202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ZTRS30FI
- Product Code / EMDN
- M0201050102,M0201050202
- Device Name
- TAMPONI DI GARZA NON STERILI
- Database Sync Date
- 2026-08-09 16:47:14
Full Regulatory Attributes
🔒 Token Gated
{
"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 TAMPONI DI GARZA NON STERILI?
The registered manufacturer of record for TAMPONI DI GARZA NON STERILI is Santex S.p.A..
What is the Primary UDI-DI identifier for TAMPONI DI GARZA NON STERILI?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08011809022553.
What classification code is assigned to this device?
This device is registered under product classification code M0201050102,M0201050202.
Similar Classification Devices (M0201050102,M0201050202)
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