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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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SentrySuite 3.30 — 2 UDI-DI variants, MDR (Jaeger Medical GmbH)

MD Atlas
Jaeger Medical GmbH

Data from EUDAMED, last updated May 23, 2026

SentrySuite 3.30

42508929012112AG3

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Jaeger Medical GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 42508929012112AG3
Device name: SentrySuite 3.30
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: May 16, 2024

Manufacturer & authorised representative

Manufacturer

Name: Jaeger Medical GmbH
SRN: DE-MF-000007090
Country: Germany
Email: jared.cardon@jaegerrdx.com
Phone: +49 931 4972 111

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HY0XZRF5M65N5WBT3E6TZMR0

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

V-77096804250892905945
V-77096804250892907345