- Role
- Country
- Date of registration
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EUDAMED last updated this device on May 16, 2026
++G006OphthalSpeculumU8Titanium Wright Spring Solid Blade Eye Speculum is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Daud Jee Mfg. Co. Placed on the EU market in Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
PK-MF-000009615+G006DT1053040W
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.
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 Spain; available across 7 countries total.
| Country | On market since | Until |
|---|---|---|
| SpainPrimary placement | Apr 20, 2021 | Apr 19, 2028 |
| Germany | Apr 20, 2021 | Apr 19, 2028 |
| France | Apr 20, 2021 | Apr 19, 2028 |
| Italy | Apr 20, 2021 | Apr 19, 2028 |
| Netherlands | Apr 20, 2021 | Apr 19, 2028 |
| Portugal | Apr 20, 2021 | Apr 19, 2028 |
| Türkiye | Apr 20, 2021 | Apr 19, 2028 |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
+G006DT1053040WBasic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
++G006OphthalSpeculumU8DT10-5304UDI 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.
L1799OPHTHALMOLOGY INSTRUMENTS, REUSABLE- OTHERPrimary 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 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.No certificate specifically references this device's Basic UDI-DI.
++G006OphthalmicScissorDSOn the marketTITANIUM Vitrectomy Scissors Horizontol str 20G++G006OphthalmicScissorDSOn the marketTITANIUM VITRECTOMY SCISSORS vertical opening str 20G++G006OphthalmicScissorDSOn the marketTITANIUM YAE SCISSORS 23 gauge 3mm blade 24mm SHAFT++G006OphthalmicScissorDSOn the marketTITANIUMJAFFE FORCEPS DEL 11MM LONG++G006OphthalmicForceps9BOn the marketTITANIUMRETINAL Eckardt End-gripping 23G++G006OphthalmicForceps9BOn the market