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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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Japet.W+ T1 — 2 UDI-DI variants, MDR (Japet Medical Devices)

MD Atlas
Japet Medical Devices

Data from EUDAMED, last updated May 19, 2026

Japet.W+ T1

3770027792Japet_0014S

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: Japet Medical Devices

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Device characteristics

Active device

Clinical investigations

Registered: No

Registered: No

Registered: No

Identity & classification

Basic UDI-DI: 3770027792Japet_0014S
Device name: Japet.W+ T1
Device model: Japet.W+ T1
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Aug 8, 2024

Manufacturer & authorised representative

Manufacturer

Name: Japet Medical Devices
SRN: FR-MF-000024278
Country: France
Email: contact@japet.eu
Phone: +33 1 88 32 10 11

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01J4RCW38V4FTFVDS74N5CCXF5

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

Japet.W+ T103770027792024
Japet.W+ T203770027792031