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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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Maniglioni Serie Inox — 7 UDI-DI variants, MDR

MD Atlas
THERMOMAT SANILINE S.R.L.

Data from EUDAMED, last updated May 30, 2026

Maniglioni Serie Inox

805534948MANNX0004E

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: THERMOMAT SANILINE S.R.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805534948MANNX0004E
Device name: Maniglioni Serie Inox
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 19, 2026

Manufacturer & authorised representative

Manufacturer

Name: THERMOMAT SANILINE S.R.L.
SRN: IT-MF-000051936
Country: Italy
Email: info@thermomat.com
Phone: +39 0376 4473

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS0291PMSMTVV4NKABDCWCHY

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

M120-NX-S08055349480824
MAD-NX-S08055349480886
SLNXMAD7150WAL08055349483139
SLNXMAN0400XAL08055349483146
SLNXMAN0400XFS08055349483153
SLNXMAN0600XFS08055349483160
SLNXMAN0800XAL08055349483177