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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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SENTRY 1200 ST SAC — 2 UDI-DI variants, MDR (MEDIDEV - SENTECH FRANCE)

MD Atlas
MEDIDEV - SENTECH FRANCE

Data from EUDAMED, last updated May 19, 2026

SENTRY 1200 ST SAC

376033037SAC1200ST1S4

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: MEDIDEV - SENTECH FRANCE

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 376033037SAC1200ST1S4
Device name: SENTRY 1200 ST SAC
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: MEDIDEV - SENTECH FRANCE
SRN: FR-MF-000008021
Country: France
Email: webmaster@sentechfrance.com
Phone: 0553405035

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KQ76HF43EBWYEV7001J8RC0V

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

SAC1200MR01B03760330371078
SAC1200MR01R03760330371061