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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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Personenversorgungskammer (PVK) — 1 UDI-DI variant, MDR (Aerolite AG)

MD Atlas
Aerolite AG

Data from EUDAMED, last updated May 31, 2026

Personenversorgungskammer (PVK)

7649996678PVKWK

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Aerolite AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7649996678PVKWK
Device name: Personenversorgungskammer (PVK)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: Aerolite AG
SRN: CH-MF-000013572
Country: Switzerland
Email: antonello.pisani@aerolite.ch
Phone: 0416245892

Authorised representative

Name: Johner Medical GmbH
SRN: DE-AR-000011832
Country: Germany

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KSQEF1YY1EXNRG2D1JECGV6J

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

006-0326374-50107640263171647