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EUDAMED last updated this device on Jul 15, 2026
B-00817122020577Footswitch, Muting is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Vascular Technology, Incorporated. Placed on the EU market in Belgium. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
US-MF-000044944HD 60145551 0001(01)00817122020577
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.
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.
Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
Primary placement in Belgium; available across 10 countries total.
| Country | On market since | Until |
|---|---|---|
| BelgiumPrimary placement | — | Still on market |
| Austria | — | Still on market |
| EL | — | Still on market |
| France | — | Still on market |
| Ireland | — | Still on market |
| Luxembourg | — | Still on market |
| Latvia | — | Still on market |
| Poland | — | Still on market |
| Romania | — | Still on market |
| Sweden | — | Still on market |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
00817122020577Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
B-00817122020577201450UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
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.
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z11040199ULTRASOUND SCANNERS - OTHERPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →B-00817122020393On the market20 MHz Micro Disposable Doppler ProbeB-10817122020222On the market8 MHz Kelly Endonasal Disposable Doppler ProbeB-10817122020277On the marketMizuho 07-150-07 Disposable Doppler Probe for Neurosurgery (20 MHZ)B-10817122020260On the marketMizuho 07-150-10 Disposable Doppler Probe for Neurosurgery (20 MHz)B-10817122020208On the marketMizuho 07-150-12 20 MHz Micro Disposable Doppler ProbeB-10817122020338On the marketNo certificate specifically references this device's Basic UDI-DI.
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.