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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

MAAM — Class I MDR by Tex Acces MCV S.R.L.

MD Atlas
Tex Acces MCV S.R.L.

EUDAMED last updated this device on Apr 2, 2026

MAAM

59447591COR6B

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Tex Acces MCV S.R.L.
UDI-DI code: 05944759123724
Reference / catalog number: CAV 35 XS

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View device family (Basic UDI)

Manufacturer information

Organization name: Tex Acces MCV S.R.L.
SRN: RO-MF-000029775
Manufacturer status: Active

Related devices

MAAM59447591MAN6BOn the market MAAM59447591MAN6BOn the market MAAM59447591MAN6BOn the market MAAM59447591COS6DOn the market MAAM59447591MAN6BOn 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.

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Romania; available across 1 country total.

Country	On market since	Until
RomaniaPrimary placement		Still on market

Device identification

Trade name: MAAM
UDI-DI code: 05944759123724
Basic UDI-DI: 59447591COR6B
Reference / catalog number: CAV 35 XS
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: ABDOMINAL BELT, ADJUSTABLE, Rigida 35 XS
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

M030499ELASTIC BANDAGES, SUPPORT AND COMPRESSION - 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

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