eudamed_udi
Primary ID: 08051277605698
MATERASSO ESTASI 100X200 CE (UDI 08051277605698)
Manufactured by TECHNOGEL ITALIA SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MATERASSO ESTASI 100X200 CE - Primary ID 08051277605698
Device Regulatory Overview
The MATERASSO ESTASI 100X200 CE (Model/Catalog Number: QE7100200EUCE) is a medical device manufactured by TECHNOGEL ITALIA SRL. This product is indexed under FDA Product Code / Category Classification V080702 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- QE7100200EUCE
- Product Code / EMDN
- V080702
- Device Name
- ESTASI
- Database Sync Date
- 2026-08-09 16:46:17
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 MATERASSO ESTASI 100X200 CE?
The registered manufacturer of record for MATERASSO ESTASI 100X200 CE is TECHNOGEL ITALIA SRL.
What is the Primary UDI-DI identifier for MATERASSO ESTASI 100X200 CE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08051277605698.
What classification code is assigned to this device?
This device is registered under product classification code V080702.
Similar Classification Devices (V080702)
Other Devices by TECHNOGEL ITALIA SRL
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