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EUDAMED last updated this device on Oct 5, 2024
8682139009CYCESSCHRODER - OT140 - OPERATION ROOM TRANSFER STRETCHER 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 Türkiye. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
8682139009660OT1408682139009660
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.
European Medical Device Nomenclature — the EU product classification assigned to this device.
V08050103EMERGENCY AND TRAUMATOLOGY STRETCHERSTR-MF-000017590Sterile
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 Türkiye; available across 1 country total.
Placed on the market in Türkiye; per-country availability dates not published.
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.
8682139009NTN9On the marketSCHRODER - NT 130 - NEGATOSCOPE, TRIPLE8682139009NTN9On the marketSCHRODER - OBT 162 - OVERBED TABLE8682139009OBT162CDOn the marketSCHRODER - PDB 1120 - TWO MOTORISED PAEDIATRIC BED8682139009PDBESOn the marketSCHRODER - PDB 1120 AL - TWO MOTOR ALUMINUM PEDIATRIC BED8682139009PDBESOn the marketSCHRODER - PDB 1120 PK - TWO MOTORIZED PEDIATRIC BED8682139009PDBESOn 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.