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EUDAMED last updated this device on Apr 23, 2024
803373771DIAS0002HCTHD LIGHT-SCOPE ANO (LED TR/ST) is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by THD S.P.A.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
080337377105318001121 packaging level registered — each level carries its own UDI-DI.
08033737710531× 1 unitBase unit18033737710538× 10 units(01)08033737710531
European Medical Device Nomenclature — the EU product classification assigned to this device.
G02060301ANOSCOPES4 warnings recorded — scroll inside the panel to see all entries.
Primary placement in Italy; available across 1 country total.
Placed on the market in Italy; per-country availability dates not published.
IT-MF-000029427The 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.
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 →803373771DIANSAC056NOn the marketTHD LIGHT-SCOPE ANO (LED BE/NS)803373771DIANS0002Y3On the marketTHD LIGHT-SCOPE ANO (LED TR/NS)803373771DIANS0002Y3On the marketTHD LIGHT-SCOPE ANO (TR/NS)803373771DIANS0001XZOn the marketTHD LIGHT-SCOPE HRA LASER803373771DIANS0003Y5On the marketTHD LIGHT-SCOPE MAXI-RECTO (INS/NS)803373771DIANS0001XZOn 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.