- Role
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EUDAMED last updated this device on May 29, 2026
081128603PVChartsLFLandolt C, (8 Direction) ETDRS Style Folding Chart for 3 meter (10 foot) Testing. is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Precision Vision, Inc.. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
US-MF-000008456(01)00811286032810
The 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.
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 Netherlands; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | — | Still on market |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
00811286032810Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
081128603PVChartsLF2204-FCUDI 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.
Z1212012099INSTRUMENTS FOR THE ASSESSMENT OF VISUAL FUNCTIONALITY - 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 certificate specifically references this device's Basic UDI-DI.
081128603PVChartsLFOn the marketLandolt C, Runge Design Pocket Near Vision Card, for testing at 40cm (16 in.)081128603PVChartsLFOn the marketLandolt C, - Near & Intermediate Vision Testing Charts | Side 1 - Near Vision for Testing at 40cm | Side 2- Intermediate Vision for Testing at 60cm081128603PVChartsLFOn the marketLandolt C, (8 Direction) One sided near point card, printed on white styrene plastic. calibrated for 80cm. An attached cord is provided for accurate viewing distance.081128603PVChartsLFOn the marketLandolt C, (8 Direction) One sided near point card, printed on white styrene plastic. calibrated for 80cm. An attached cord is provided for accurate viewing distance. SCRAMBLED VERSION A081128603PVChartsLFOn the marketLandolt C, (8 Direction) Two sided near point card, printed on white styrene plastic. calibrated for 100cm. An attached cord is provided for accurate viewing distance.081128603PVChartsLFOn the marketNo 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.