- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Sep 11, 2026
709000879TS101106C8Redcord Tandem Station is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by REDCORD AS. Placed on the EU market in Norway. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
07090008790686101106-2(01)07090008790686
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z120603PASSIVE REHABILITATIVE GYMNASTICS EQUIPMENTPrimary placement in Norway; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| NorwayPrimary placement | — | Still on market |
NO-MF-000014649The 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.
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 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.709000879SLINGSS111003ZDOn the marketRedcord Strap, one pair709000879STRAP111200RAOn the marketRedcord Tandem Station709000879TS101106C8On the marketRedcord Trainer709000879TR110010BDOn the marketRedcord Wide sling709000879SLINGW111001NJOn the marketRedcord Workstation Professional709000879WSP1000233POn the marketNo certificate specifically references this device's Basic UDI-DI.