- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Aug 6, 2026
B-08717872003122Forceps for removal of cannulas is an MDD-legacy medical device registered in EUDAMED. It is classified as Class I. Manufactured by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
087178720031221278(01)08717872003122
European Medical Device Nomenclature — the EU product classification assigned to this device.
L170299OPHTHALMOLOGY FORCEPS, REUSABLE - OTHER1 warning recorded — scroll inside the panel to see all entries.
NL-MF-000015696No 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.Primary placement in Netherlands; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | — | Still on market |
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.
B-08717872006437On the marketExtendible diamond dusted sweeper (25 gauge / 0.5 mm)B-08717872020556On the marketFeatherlight micro Phaco emulsification/fragmentation handpieceB-08717872008899On the marketHigh flow infusion line for 20, 23, 25 & 27G cannula systemB-08717872018546On the marketHigh flow viscous fluid extraction accessory Compatible with EVA AVETA: 1272.ED23/25/27, 1272.EDH23/25, 1272.EDPP23/25/27, 1272.ED223B-08717872033105On the marketHigh Flow Viscous Fluid Extraction Suitable for 20/23/25/27G DORC Cannula SystemsB-08717872019628On the market