- Role
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EUDAMED last updated this device on May 27, 2026
08402216STRIPINT42Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →OSS-37F-MS is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Microcopy, A Division of Neo-Flo, Inc.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
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 →00840221637773Basic 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 →08402216STRIPINT42OSS-37F-MSUDI 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 →(01)00840221637773
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
Q019003DENTAL FLOSS AND OTHER DEVICES FOR ORAL HYGIENE (FOR PROFESSIONAL USE)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 →No certificate specifically references this device's Basic UDI-DI.
Primary placement in Germany; available across 31 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Jan 1, 2024 | Still on market |
| Austria | Jan 1, 2024 | Still on market |
| Belgium | Jan 1, 2024 | Still on market |
| Bulgaria | Jan 1, 2024 | Still on market |
| Cyprus | Jan 1, 2024 | Still on market |
| Czechia | Jan 1, 2024 | Still on market |
| Denmark | Jan 1, 2024 | Still on market |
| Estonia | Jan 1, 2024 | Still on market |
| EL | Jan 1, 2024 | Still on market |
| Spain | Jan 1, 2024 | Still on market |
| Finland | Jan 1, 2024 | Still on market |
| France | Jan 1, 2024 | Still on market |
| Croatia | Jan 1, 2024 | Still on market |
| Hungary | Jan 1, 2024 | Still on market |
| Ireland | Jan 1, 2024 | Still on market |
| Iceland | Jan 1, 2024 | Still on market |
| Italy | Jan 1, 2024 | Still on market |
| Liechtenstein | Jan 1, 2024 | Still on market |
| Lithuania | Jan 1, 2024 | Still on market |
| Luxembourg | Jan 1, 2024 | Still on market |
| Latvia | Jan 1, 2024 | Still on market |
| Malta | Jan 1, 2024 | Still on market |
| Netherlands | Jan 1, 2024 | Still on market |
| Norway | Jan 1, 2024 | Still on market |
| Poland | Jan 1, 2024 | Still on market |
| Portugal | Jan 1, 2024 | Still on market |
| Romania | Jan 1, 2024 | Still on market |
| Sweden | Jan 1, 2024 | Still on market |
| Slovenia | Jan 1, 2024 | Still on market |
| Slovakia | Jan 1, 2024 | Still on market |
| Türkiye | Jan 1, 2024 | Still on market |
US-MF-000012637No 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.