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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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Speculum auricolari Hartmann — 4 UDI-DI variants, MDR

MD Atlas
AIESI HOSPITAL SERVICE S.a.s. di PIANTADOSI VALERIO E C

Data from EUDAMED, last updated May 31, 2026

Speculum auricolari Hartmann

805228320L149004LG

4 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: AIESI HOSPITAL SERVICE S.a.s. di PIANTADOSI VALERIO E C

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 805228320L149004LG
Device name: Speculum auricolari Hartmann
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 3, 2025

Manufacturer & authorised representative

Manufacturer

Name: AIESI HOSPITAL SERVICE S.a.s. di PIANTADOSI VALERIO E C
SRN: IT-MF-000032617
Country: Italy
Email: COMMERCIALE@AIESI.IT
Phone: +39 081267536

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01JZ7GRVG62TTJ621WZ3Q9997J

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

SBA-141-270218052283204933
SBA-147-283218052283206661
SBA-147-283018052283205169
SBA-147-283118052283206654