eudamed_udi
Primary ID: 03760330371160
SENTRY M1200MR02 (UDI 03760330371160)
Manufactured by MEDIDEV - SENTECH FRANCE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SENTRY M1200MR02 - Primary ID 03760330371160
Device Regulatory Overview
The SENTRY M1200MR02 (Model/Catalog Number: M1200MR02) is a medical device manufactured by MEDIDEV - SENTECH FRANCE. This product is indexed under FDA Product Code / Category Classification V080701 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- M1200MR02
- Product Code / EMDN
- V080701
- Device Name
- SENTRY 1200 ST Mattress
- Database Sync Date
- 2026-08-09 16:45:37
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 SENTRY M1200MR02?
The registered manufacturer of record for SENTRY M1200MR02 is MEDIDEV - SENTECH FRANCE.
What is the Primary UDI-DI identifier for SENTRY M1200MR02?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03760330371160.
What classification code is assigned to this device?
This device is registered under product classification code V080701.
Similar Classification Devices (V080701)
Other Devices by MEDIDEV - SENTECH FRANCE
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