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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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PM2-A MIS — 4 UDI-DI variants, MDR (Bien-Air Surgery SA)

MD Atlas
Bien-Air Surgery SA

Data from EUDAMED, last updated May 23, 2026

PM2-A MIS

76300555_009_FG

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Bien-Air Surgery SA

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 76300555_009_FG
Device name: PM2-A MIS
Device model: PM2 Handpieces
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: Bien-Air Surgery SA
SRN: CH-MF-000016376
Country: Switzerland
Email: surgery@bienair.com

Authorised representative

Name: Bien-Air Europe Sàrl
SRN: FR-AR-000011942
Country: France

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KG4FW6QDH0RQVRSZWA1R4PK3

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

160102707630055508065
150237507630055508096
150293807630055512604
160102807630055508072