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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

Cupule XLmob sans ciment Ø 50 mm… — Class III MDR

MD Atlas
PROTHEOS INDUSTRIE

EUDAMED last updated this device on Sep 25, 2025

Cupule XLmob sans ciment Ø 50 mm (XX)

++EPRS15040000BUH

On the marketClass III

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: PROTHEOS INDUSTRIE
UDI-DI code: EPRS1504XX50B0
Reference / catalog number: 15-04-XX-50

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Manufacturer information

Organization name: PROTHEOS INDUSTRIE
SRN: FR-MF-000000150
Manufacturer status: Active

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Critical warnings

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

CW009
EUDAMED did not publish a description for this code.
CW001
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW011
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW026
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	Feb 27, 2017	Still on market

Device identification

Trade name: Cupule XLmob sans ciment Ø 50 mm (XX)
UDI-DI code: EPRS1504XX50B0
Basic UDI-DI: ++EPRS15040000BUH
Reference / catalog number: 15-04-XX-50
Issuing entity: HIBCC

Classification

Risk category: Class III
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)

P090803050102UNCEMENTED DOUBLE-MOBILITY ACETABULAR CUPS

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

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Expiration date
Manufacturing date
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Software identification