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EUDAMED last updated this device on Mar 19, 2025
8712175_TD_11_SPSUPFS7751 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Bevaplast B.V.. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
087121759363207751(01)08712175936320
European Medical Device Nomenclature — the EU product classification assigned to this device.
M030499ELASTIC BANDAGES, SUPPORT AND COMPRESSION - OTHER3 warnings recorded — scroll inside the panel to see all entries.
ISO symbol
ISO symbol, Do not use on inflamed, injured or bleeding skin. If a numb or tingling sensation sets in, remove the bandage immediately and check that it is the right size. Do not wear the bandage for long periods of time (no longer than 2 hours continuously, or 6 hours per day) and not while sleeping. For sensory disorders of the skin, circulatory and lymphatic drainage disorders and skin diseases consult a doctor before use. Do not use the support in combination with other compression products, creams, skin oils, etc. Consult a doctor if you have questions about the injury or if the symptoms persist or worsen. In isolated cases, skin reactions or irritations may occur. If these persist, stop wearing the bandage and consult a doctor if necessary. Discontinue use if if the elasticity of the bandage decreases. Inform the manufacturer and the competent authority about serious incidents.
OTHER
Primary placement in Netherlands; available across 5 countries total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | Oct 2, 2023 | Still on market |
| Austria | Oct 2, 2023 | Still on market |
| Germany | Oct 2, 2023 | Still on market |
| Croatia | Jan 14, 2026 | Still on market |
| Slovakia | Oct 2, 2023 | Still on market |
NL-MF-000004386The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
View in glossary →Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
View in glossary →Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
View in glossary →CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
View in glossary →Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →No certificate specifically references this device's Basic UDI-DI.
Certificate health across this manufacturer's portfolio.
2265082CE01IssuedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →