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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

CALIMA — Class I MDR by Celsius Medical S.L.

MD Atlas
Celsius Medical S.L.

EUDAMED last updated this device on May 28, 2026

CALIMA

8433839CSBHF

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Celsius Medical S.L.
UDI-DI code: 18433839920130
Reference / catalog number: CSOCA1

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View device family (Basic UDI)

Manufacturer information

Organization name: Celsius Medical S.L.
SRN: ES-MF-000006604
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement	Nov 17, 2025	Still on market

Device identification

Trade name: CALIMA
UDI-DI code: 18433839920130
Basic UDI-DI: 8433839CSBHF
Reference / catalog number: CSOCA1
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: Sterile convective air blankets for prevention of perioperative hypothermia of the patient.
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)18433839920130

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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.

T030301AIR FLOW BLANKETS

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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Related devices

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Certificates

Certificate health across this manufacturer's portfolio.

ES25/00001195Issued
Quality management systemNotified body: 1639Expiry: Nov 17, 2030