eudamed_udi
Primary ID: 03760330371085
SENTRY MD98000120 (UDI 03760330371085)
Manufactured by MEDIDEV - SENTECH FRANCE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SENTRY MD98000120 - Primary ID 03760330371085
Device Regulatory Overview
The SENTRY MD98000120 (Model/Catalog Number: MD98000120) is a medical device manufactured by MEDIDEV - SENTECH FRANCE. This product is indexed under FDA Product Code / Category Classification Z12030102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MD98000120
- Product Code / EMDN
- Z12030102
- Device Name
- SENTRY 1200 ST
- Database Sync Date
- 2026-08-09 16:29:51
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 MD98000120?
The registered manufacturer of record for SENTRY MD98000120 is MEDIDEV - SENTECH FRANCE.
What is the Primary UDI-DI identifier for SENTRY MD98000120?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03760330371085.
What classification code is assigned to this device?
This device is registered under product classification code Z12030102.
Similar Classification Devices (Z12030102)
Other Devices by MEDIDEV - SENTECH FRANCE
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