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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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Organization name
UDI-DI code
Reference / catalog number

LM Neonatal Testlung, Disposable — Class I MDR

MD Atlas
Löwenstein Medical SE & Co. KG

EUDAMED last updated this device on Dec 3, 2025

LM Neonatal Testlung, Disposable

426017127TestlungL8

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Löwenstein Medical SE & Co. KG
UDI-DI code: 04260171276345
Reference / catalog number: 0217043v01bg

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Manufacturer information

Organization name: Löwenstein Medical SE & Co. KG
SRN: DE-MF-000006028
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Placed on the market in Germany; per-country availability dates not published.

Device identification

Trade name: LM Neonatal Testlung, Disposable
UDI-DI code: 04260171276345
Basic UDI-DI: 426017127TestlungL8
Reference / catalog number: 0217043v01bg
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z1203010580PULMONARY VENTILATORS FOR HOSPITAL USE - HARDWARE ACCESSORIES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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Certificates

Certificate health across this manufacturer's portfolio.

HZ 1011391-1Issued
Quality management systemNotified body: 0197Expiry: Sep 5, 2028