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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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LEMI — 43 UDI-DI variants, MDR (Brusaferri & C. srl)

MD Atlas
Brusaferri & C. srl

Data from EUDAMED, last updated May 30, 2026

LEMI

805686022851FA

43 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: Brusaferri & C. srl

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UDI-DI variants

43 UDI-DI variants

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Applied filters

basicUdiUlid01HNMZHWCQPRET86FR9NCXAZM3

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

002 - WELL80568602203572
1126 - SOSUL80568602203336
1127 - SOSUL 200080568602203268
ABOUT LEMI 202480568602200984
ABOUT LEMI 202480568602202346
ABOUT LEMI 202480568602200366
1142 - SOMED80568602203404
1155 - SOSUL TOP 3M80568602203022
1157 DREAMED ZAK 4M MOVE80568602201592
ABOUT LEMI 202480568602200434
ABOUT LEMI 202480568602202032
ABOUT LEMI 202480568602200502
ABOUT LEMI 202480568602201806
1167 - SOSUL TOP 2M80568602203190
ABOUT LEMI 202480568602202582
ABOUT LEMI 202480568602202650
ABOUT LEMI 202480568602201288
ABOUT LEMI 202480568602201110
ABOUT LEMI 202480568602201042
ABOUT LEMI 202480568602201424
ABOUT LEMI 202480568602201356
ABOUT LEMI 202480568602200816
ABOUT LEMI 202480568602201660
ABOUT LEMI 202480568602201738
ABOUT LEMI 202480568602202278

1 2

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805686022851FA
Device name: LEMI
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 2, 2024

Manufacturer & authorised representative

Manufacturer

Name: Brusaferri & C. srl
SRN: IT-MF-000039891
Country: Italy
Email: info@lemigroup.it
Phone: +39 0374363069

Variants by status