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US-MF-000009087Rainbow Epi Flex Resistance Bar, Level 2 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by North Coast Medical Inc.. Placed on the EU market in Austria. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Jul 7, 2026
0768627REHAB-4412FLPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)00768627016742
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 Austria; available across 11 countries total.
| Country | On market since | Until |
|---|---|---|
| AustriaPrimary placement | Jul 15, 2026 | Still on market |
| Belgium | Jul 15, 2026 | Still on market |
| Germany | Jul 15, 2026 | Still on market |
| Denmark | Jul 15, 2026 | Still on market |
| Spain | Jul 15, 2026 | Still on market |
| Finland | Jul 15, 2026 | Still on market |
| France | Jul 15, 2026 | Still on market |
| Ireland | Jul 15, 2026 | Still on market |
| Luxembourg | Jul 15, 2026 | Still on market |
| Sweden | Jul 15, 2026 | Still on market |
| XI | Jul 15, 2026 | 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.
00768627016742Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
0768627REHAB-4412FLNC16511UDI 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.
Z120616ELECTROMECHANICAL SYSTEMS FOR PHYSICAL THERAPYNo 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.0768627REHAB-4410-RYOn the marketRainbow0768627REHAB-4410-RYOn the marketRainbow Epi Flex Resistance Bar, Level 10768627REHAB-4412FLOn the marketRainbow Epi Flex Resistance Bar, Level 30768627REHAB-4412FLOn the marketRainbow Epi Flex Resistance Bar, Level 40768627REHAB-4412FLOn the marketRainbow Epi Flex Resistance Bar, Level 50768627REHAB-4412FLOn the market