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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

Housse pour amplificateur de… — Class I MDR by CG MEDICAL

MD Atlas
CG MEDICAL

EUDAMED last updated this device on Apr 15, 2026

Housse pour amplificateur de brillance - 150x270cm - Stérile / Protection Emetteur/Recepteur

37014200HOUPESTE01RF

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: CG MEDICAL
UDI-DI code: 03701420005749
Reference / catalog number: PR-AMPC1527

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Manufacturer information

Organization name: CG MEDICAL
SRN: FR-MF-000001721
Manufacturer status: Active

Critical warnings

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

CW032
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW001
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Oct 6, 2004	Still on market

Device identification

Trade name: Housse pour amplificateur de brillance - 150x270cm - Stérile / Protection Emetteur/Recepteur
UDI-DI code: 03701420005749
Basic UDI-DI: 37014200HOUPESTE01RF
Reference / catalog number: PR-AMPC1527
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)

T030199COVERS, INSTRUMENTS AND EQUIPMENT - OTHER

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

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.

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