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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

LifePipe — Class I MDR by CNSAC MedShop GmbH

MD Atlas
CNSAC MedShop GmbH

EUDAMED last updated this device on Mar 16, 2026

LifePipe

426235615HC014H

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: CNSAC MedShop GmbH
UDI-DI code: 04262356152109
Reference / catalog number: LP301

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Manufacturer information

Organization name: CNSAC MedShop GmbH
SRN: DE-MF-000024329
Manufacturer status: Active

Related devices

CNSAC426235615NC0767On the market CNSAC426235615NC0767On the market CNSAC426235615NC0767On the market CNSAC426235615NC0767On the market CNSAC426235615NC0563On the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

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: LifePipe
UDI-DI code: 04262356152109
Basic UDI-DI: 426235615HC014H
Reference / catalog number: LP301
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: LifePipe: Portable Respiratory Therapy Device for Use During All Daily Activities
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

R900902INSPIRATORY AND EXPIRATORY FLOW STIMULATORS/RESPIRATORY MUSCLES TRAINERS

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
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Software identification