eudamed_udi
Primary ID: 03760330371061
SENTRY SAC1200MR01R (UDI 03760330371061)
Manufactured by MEDIDEV - SENTECH FRANCE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SENTRY SAC1200MR01R - Primary ID 03760330371061
Device Regulatory Overview
The SENTRY SAC1200MR01R (Model/Catalog Number: SAC1200MR01R) is a medical device manufactured by MEDIDEV - SENTECH FRANCE. This product is indexed under FDA Product Code / Category Classification T0399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SAC1200MR01R
- Product Code / EMDN
- T0399
- Device Name
- SENTRY 1200 ST SAC
- Database Sync Date
- 2026-08-09 17:01:42
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 SENTRY SAC1200MR01R?
The registered manufacturer of record for SENTRY SAC1200MR01R is MEDIDEV - SENTECH FRANCE.
What is the Primary UDI-DI identifier for SENTRY SAC1200MR01R?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03760330371061.
What classification code is assigned to this device?
This device is registered under product classification code T0399.
Similar Classification Devices (T0399)
Other Devices by MEDIDEV - SENTECH FRANCE
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