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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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Bliss DTx — 3 UDI-DI variants, MDR (Butterfly Therapeutics)

MD Atlas
Butterfly Therapeutics

Data from EUDAMED, last updated May 19, 2026

Bliss DTx

3770031579BlissDTX9Y

3 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: Butterfly Therapeutics

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 3770031579BlissDTX9Y
Device name: Bliss DTx
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Special device type: refdata.special-mdr-device-type.software
Version date: Dec 14, 2023

Manufacturer & authorised representative

Manufacturer

Name: Butterfly Therapeutics
SRN: FR-MF-000036923
Country: France
Email: contact@bliss-dtx.com
Phone: +33767120602

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HHN13JSN9QR9XCSN4J0MAEW9

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

0377003157903103770031579031
377003157904803770031579048
0377003157902403770031579024