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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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SOCRATES — 1 UDI-DI variant, MDD (Hedera Biomedics S.r.l.)

MD Atlas
Hedera Biomedics S.r.l.

Data from EUDAMED, last updated May 30, 2026

SOCRATES

B-805714366SCR001AVNQ

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class I

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Manufacturer: Hedera Biomedics S.r.l.

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Device characteristics

Active deviceMeasuring function

Legacy certificates

Certificate number: MED31241
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: KIWA CERMET ITALIA S.P.A. (0476)
Validity: May 26, 2024

Identity & classification

Basic UDI-DI: B-805714366SCR001AVNQ
Device name: SOCRATES
Device model: SOCRATES BASE
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Version date: Jan 30, 2024

Manufacturer & authorised representative

Manufacturer

Name: Hedera Biomedics S.r.l.
SRN: IT-MF-000039831
Country: Italy
Email: dehesh@hederabiomedics.com
Phone: +39 3282346771

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01HNDMBMV7FP8QTXR0PTE5V5DT

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

SCR.001D-805714366SCR001AVNQ