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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

Bouillotte Sèche Calin — Class I MDR by MG MICALLEF

MD Atlas
MG MICALLEF

EUDAMED last updated this device on Apr 16, 2026

Bouillotte Sèche Calin

37700419320003KZ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MG MICALLEF
UDI-DI code: 37700419320310
Reference / catalog number: Bouillotte Sèche Calin

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Manufacturer information

Organization name: MG MICALLEF
SRN: FR-MF-000052601
Manufacturer status: Active

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Apr 16, 2026	Still on market

Device identification

Trade name: Bouillotte Sèche Calin
UDI-DI code: 37700419320310
Basic UDI-DI: 37700419320003KZ
Reference / catalog number: Bouillotte Sèche Calin
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)

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

Bouillotte Sèche Cervicale37700419320001KVOn the market Bouillotte Sèche Dorsale37700419320002KXOn the market Bouillotte Sèche Dualtherm37700419320004L3On the market Bouillotte Sèche Mini37700419320005L5On 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.