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EUDAMED last updated this device on Aug 17, 2023
B-08719934000247Ryder Regular is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Medical-Latex (DUA) Sdn. Bhd.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
MY-MF-000001244CE 664546(01)08719934000247
5 warnings recorded — scroll inside the panel to see all entries.
Do not use the condom if the rubber materials are sticky or brittle. If the individual container is obviously damaged, discard that condom and use a new one from an undamaged package.
Condoms are for single use only; reused condom could increase the risk of breakage and infection.
Read carefully the instructions before use.
This product contains natural rubber latex which may cause allergic reactions including anaphylactic shock. If you are allergic to natural rubber latex products, consult your doctor for advice before use
Consult a doctor or a pharmacist if you or your partner is using prescription or over-the-counter medication that is applied to the penis or vagina and may come into contact with the condom.
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 Germany; available across 10 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | — | Apr 25, 2023 |
| Bulgaria | — | Apr 25, 2023 |
| Czechia | — | Apr 25, 2023 |
| Spain | — | Apr 25, 2023 |
| France | — | Apr 25, 2023 |
| Hungary | — | Apr 25, 2023 |
| Italy | — | Apr 25, 2023 |
| Netherlands | — | Apr 25, 2023 |
| Poland | — | Apr 25, 2023 |
| Slovakia | — | Apr 25, 2023 |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
08719934000247Basic 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-08719934000247C53SC-N1UDI 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.
U110101CONDOMSPrimary 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.
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.