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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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EmbracePlus — 4 UDI-DI variants, MDR (Empatica S.r.L.)

MD Atlas
Empatica S.r.L.

Data from EUDAMED, last updated May 30, 2026

EmbracePlus

0853858006EMBRACEPLUS44

4 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: Empatica S.r.L.

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Device characteristics

Active deviceMeasuring function

Clinical investigations

Investigation number: NCT04964609
Registered: No
Countries: United States

Investigation number: NCT04897529
Registered: No
Countries: United States

Investigation number: NCT05701761
Registered: No
Countries: United States

Identity & classification

Basic UDI-DI: 0853858006EMBRACEPLUS44
Device name: EmbracePlus
Device model: EmbracePlus
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 11, 2024

Manufacturer & authorised representative

Manufacturer

Name: Empatica S.r.L.
SRN: IT-MF-000012905
Country: Italy
Email: info@empatica.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01JCD9WTC4S04XA3KE8CB66DFK

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

EMBP-CC-MS00853858006232
EBP2-1G-FB-B00853858006584
EBP2-1G-ES-F00853858006751
EBP2-1G-SB-W00853858006546