- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Oct 31, 2025
590761904010EL1273 ORBI-FLEX 278353, 2m is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by AnGer G&A Przedsiębiorstwo Produkcyjne. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
059076190435491273 ORBI-FLEX 278353(01)05907619043549
European Medical Device Nomenclature — the EU product classification assigned to this device.
Q019003DENTAL FLOSS AND OTHER DEVICES FOR ORAL HYGIENE (FOR PROFESSIONAL USE)4 warnings recorded — scroll inside the panel to see all entries.
PL-MF-000001898The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Primary placement in Germany; available across 1 country total.
Placed on the market in Germany; per-country availability dates not published.
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.
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.590761904013ESOn the marketTransparent Light-Conductive Interdental Wedges - size Extra Extra Large, 100pcs590761904013ESOn the market1271 ORBI-FLEX 278352, 2m590761904010ELOn the market1275 ORBI-FLEX 278354, 2m590761904010ELOn the market1277 ORBI-FLEX 278355, 2m590761904010ELOn the marketAnGer G&A Polyester Crown Forms, 112pcs Pediatric590761904001EKOn the market