- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Oct 5, 2024
8682139009SCHFJSCHRODER - SCH 3060 - THREE MOTORIZED ELECTRONIC PATIENT BED is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by PROMA MEDIKAL LTD ŞTI. Placed on the EU market in Lithuania. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
8682139009585SCH 3060TR-MF-0000175908682139009585
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 Lithuania; available across 1 country total.
Placed on the market in Lithuania; per-country availability dates not published.
European Medical Device Nomenclature — the EU product classification assigned to this device.
V08060101HOSPITAL/HOME CARE ELECTRIC MEDICAL BEDSPrimary 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 →8682139009SCHFJOn the marketSCHRODER - SCH 3050 - THREE MOTORISED PATIENT BED8682139009SCHFJOn the marketSCHRODER - SCH 3050 AL - THREE MOTORIZED ALUMINUM ELECTRONIC PATIENT BED8682139009SCHFJOn the marketSCHRODER - SCH 3060 AL - THREE MOTORIZED ALUMINUM ELECTRONIC PATIENT BED8682139009SCHFJOn the marketSCHRODER - SCH 4040 - FOUR MOTORISED ELECTRONIC PATIENT BED8682139009SCHFJOn the marketSCHRODER - SCH 4040 AK - FOUR MOTORIZED ELECTRONIC ALUMINUM PATIENT BED8682139009SCHFJOn 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.