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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

8404 — Class I MDR by Bevaplast B.V.

MD Atlas
Bevaplast B.V.

EUDAMED last updated this device on Jul 22, 2025

8404

8712175_TD_09_STRXXLX

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Bevaplast B.V.
UDI-DI code: 08712175939666
Reference / catalog number: 8404

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View device family (Basic UDI)

Manufacturer information

Organization name: Bevaplast B.V.
SRN: NL-MF-000004386
Manufacturer status: Active

Related devices

91178712175_TD_11_SPSUPFSOn the market 91268712175_TD_11_SPSUPFSOn the market 91158712175_TD_11_SPSUPFSOn the market 92398712175_TD_09_STRXXLXOn the market 8590 / 87168712175_TD_11_BRACE57On the market

Certificates

Certificate health across this manufacturer's portfolio.

2265082CE01Issued
Quality assuranceNotified body: 0344Expiry: May 1, 2028

Critical warnings

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

CW009
EUDAMED did not publish a description for this code.
CW011
Consult a docter in case of skin irritation or infection. Do not re-use plaster as this can lead to infection.

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Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Jul 14, 2025	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08712175939666
Basic UDI-DI: 8712175_TD_09_STRXXLX
Reference / catalog number: 8404
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: 12
Additional product description: Wound plaster silicone non-woven assorted, 20x57 mm, 19x72 mm, 25x72 mm
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.

M0599MEDICAL PLASTERS - 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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