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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

GE-2350L-120 — Class I MDR by Kanmed AB

MD Atlas
Kanmed AB

EUDAMED last updated this device on May 29, 2026

GE-2350L-120

7350045123533131325

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Kanmed AB
UDI-DI code: 07350045122520
Reference / catalog number: GE-2350L-120

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View device family (Basic UDI)

Manufacturer information

Organization name: Kanmed AB
SRN: SE-MF-000001839
Manufacturer status: Active

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NA420001/1735004512422914132XOn the market NA420002/1735004512422914132XOn the market BB10273500451230301313WCOn the market BB30273500451230301313WCOn the market BB40273500451230301313WCOn the market

Certificates

Certificate health across this manufacturer's portfolio.

28620221903Issued
Quality management systemNotified body: 2862Expiry: Jun 9, 2030

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Sweden; available across 1 country total.

Country	On market since	Until
SwedenPrimary placement	Oct 12, 2018	Still on market

Device identification

Trade name: not provided
UDI-DI code: 07350045122520
Basic UDI-DI: 7350045123533131325
Reference / catalog number: GE-2350L-120
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.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)07350045122520

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

A030105FLUIDS HEATING SYSTEMS

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

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