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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

BC10-0018 — Class I MDR by BrainCool AB

MD Atlas
BrainCool AB

EUDAMED last updated this device on Apr 22, 2026

BC10-0018

7350135110026S

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: BrainCool AB
UDI-DI code: 07350135110116
Reference / catalog number: BC10-0018

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View device family (Basic UDI)

Manufacturer information

Organization name: BrainCool AB
SRN: SE-MF-000005547
Manufacturer status: Active

Related devices

BrainCool SystemB-07350135110130On the market BC10-00117350135110026SOn the market BC10-00137350135110026SOn the market BC10-00127350135110026SOn the market BC10-00107350135110026SOn the market

Critical warnings

3 warnings recorded — scroll inside the panel to see all entries.

CW009
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW011
EUDAMED did not publish a description for this code.

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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: not provided
UDI-DI code: 07350135110116
Basic UDI-DI: 7350135110026S
Reference / catalog number: BC10-0018
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: Soft silicone Cooling Pads [EN]
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 50–120 MU29

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)07350135110116

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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.

M9001CRYOTHERAPY AND THERMOTHERAPY DEVICES

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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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.