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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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LETTI MEDICI ELETTRICI — 7 UDI-DI variants, MDR (GARDHEN BILANCE)

MD Atlas
GARDHEN BILANCE

Data from EUDAMED, last updated May 31, 2026

LETTI MEDICI ELETTRICI

805771740LETNC

7 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: GARDHEN BILANCE

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805771740LETNC
Device name: LETTI MEDICI ELETTRICI
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 22, 2025

Manufacturer & authorised representative

Manufacturer

Name: GARDHEN BILANCE
SRN: IT-MF-000013019
Country: Italy
Email: info@gardhenbilance.it

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01K5RZ3NBNB6E904VBEHXW8EYX

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

N.A.08057717400397
N/A08057717400359
N/A08057717400809
269181108057717401110
N/A08057717400953
242994908057717400373
3487008057717400380