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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

QRX ADAPTERS — Class I MDR by AQUALEG

MD Atlas
AQUALEG

EUDAMED last updated this device on May 26, 2025

QRX ADAPTERS

3665988ADAPTATEURBB

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: AQUALEG
UDI-DI code: 03665988000007
Reference / catalog number: T-TC-PF-DH

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Manufacturer information

Organization name: AQUALEG
SRN: FR-MF-000004676
Manufacturer status: Active

Market distribution

Primary placement in France; available across 1 country total.

Placed on the market in France; per-country availability dates not published.

Device identification

Trade name: QRX ADAPTERS
UDI-DI code: 03665988000007
Basic UDI-DI: 3665988ADAPTATEURBB
Reference / catalog number: T-TC-PF-DH
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: Tube-clamp adapter with female pyramid in titanium and slots for water resist
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y062415TRANSFEMORAL PROSTHESES (FOR AMPUTATION ABOVE KNEE)
Y062409TRANSTIBIAL PROSTHESES (FOR AMPUTATION UNDER KNEE)

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

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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.