- Role
- Country
- Date of registration
- Address
BE-MF-000000691No 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.Micro-Touch Blue Nitrile is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Ansell Healthcare Europe NV. Placed on the EU market in Belgium. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Sep 28, 2023
5414566MF92134DKPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)25414566410651
The 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.
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 32 countries total.
| Country | On market since | Until |
|---|---|---|
| BelgiumPrimary placement | Jan 10, 2022 | Still on market |
| Austria | Jan 10, 2022 | Still on market |
| Bulgaria | Jan 10, 2022 | Still on market |
| Cyprus | Jan 10, 2022 | Still on market |
| Czechia | Jan 10, 2022 | Still on market |
| Germany | Jan 10, 2022 | Still on market |
| Denmark | Jan 10, 2022 | Still on market |
| Estonia | Jan 10, 2022 | Still on market |
| EL | Jan 10, 2022 | Still on market |
| Spain | Jan 10, 2022 | Still on market |
| Finland | Jan 10, 2022 | Still on market |
| France | Jan 10, 2022 | Still on market |
| Croatia | Jan 10, 2022 | Still on market |
| Hungary | Jan 10, 2022 | Still on market |
| Ireland | Jan 10, 2022 | Still on market |
| Iceland | Jan 10, 2022 | Still on market |
| Italy | Jan 10, 2022 | Still on market |
| Liechtenstein | Jan 10, 2022 | Still on market |
| Lithuania | Jan 10, 2022 | Still on market |
| Luxembourg | Jan 10, 2022 | Still on market |
| Latvia | Jan 10, 2022 | Still on market |
| Malta | Jan 10, 2022 | Still on market |
| Netherlands | Jan 10, 2022 | Still on market |
| Norway | Jan 10, 2022 | Still on market |
| Poland | Jan 10, 2022 | Still on market |
| Portugal | Jan 10, 2022 | Still on market |
| Romania | Jan 10, 2022 | Still on market |
| Sweden | Jan 10, 2022 | Still on market |
| Slovenia | Jan 10, 2022 | Still on market |
| Slovakia | Jan 10, 2022 | Still on market |
| Türkiye | Jan 10, 2022 | Still on market |
| XI | Jan 10, 2022 | 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.
25414566410651Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
5414566MF92134DK313041065 SUDI 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.
1 packaging level registered — each level carries its own UDI-DI.
25414566410651× 200 unitsBase unit35414566460653× 10 unitsEuropean Medical Device Nomenclature — the EU product classification assigned to this device.
T01020204NITRILE EXAMINATION / TREATMENT GLOVES5414566MTA553REOn the marketMicro-Touch Blue Nitrile5414566MF92134DKOn the marketMicro-Touch Blue Nitrile5414566MF92134DKOn the marketMicro-Touch Blue Nitrile5414566MF92134DKOn the marketMicro-Touch Blue Nitrile5414566MF92134DKOn the marketMicro-Touch Coated5414566MTCT553WBOn the marketNo certificate specifically references this device's Basic UDI-DI.