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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

MICROFIBER SHADES for women — Class I MDR by SIGVARIS AG

MD Atlas
SIGVARIS AG

EUDAMED last updated this device on May 22, 2026

MICROFIBER SHADES for women

7611711MFSwomen25

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SIGVARIS AG
UDI-DI code: 07613378053092
Reference / catalog number: 308124

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View device family (Basic UDI)

Manufacturer information

Organization name: SIGVARIS AG
SRN: CH-MF-000015565
Manufacturer status: Active

Related devices

Active MASCULINE7611711AMABXOn the market Active MASCULINE7611711AMABXOn the market Active MASCULINE7611711AMABXOn the market Active MASCULINE7611711AMABXOn the market Active MASCULINE7611711AMABXOn 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

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: MICROFIBER SHADES for women
UDI-DI code: 07613378053092
Basic UDI-DI: 7611711MFSwomen25
Reference / catalog number: 308124
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.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)07613378053092

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

M030405COMPRESSION STOCKINGS

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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