- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Oct 16, 2025
0768627REHAB-699-H9US-MF-000009087(01)00768627701426
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 Ireland; available across 10 countries total.
| Country | On market since | Until |
|---|---|---|
| IrelandPrimary placement | Nov 11, 2024 | Still on market |
| Austria | Nov 11, 2024 | Still on market |
| Belgium | Nov 11, 2024 | Still on market |
| Germany | Nov 11, 2024 | Still on market |
| Spain | Nov 11, 2024 | Still on market |
| Finland | Nov 11, 2024 | Still on market |
| France | Nov 11, 2024 | Still on market |
| Luxembourg | Nov 11, 2024 | Still on market |
| Sweden | Nov 11, 2024 | Still on market |
| XI | Nov 11, 2024 | 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.
00768627701426Basic 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-699-H9NC70142UDI 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.
Z12062680DYNAMOMETRIC SYSTEMS FOR MOVEMENT ANALYSIS - HARDWAREExacta Hydraulic Hand Dynamometer 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 Ireland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
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.0768627REHAB-1275-RWOn the marketExacta Evaluation Kit0768627REHAB-1656-SKOn the marketExacta Goniometer 1800768627REHAB-1273-RQOn the marketExacta Hydraulic Pinch Gauge0768627REHAB-696-GYOn the marketExacta Inclinometer0768627REHAB-4001-R2On the marketExacta International Goniometer 3600768627REHAB-3394-T2On the marketNo certificate specifically references this device's Basic UDI-DI.