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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

K-Push — Class I MDD by KINVENT Biomecanique

MD Atlas
KINVENT Biomecanique

EUDAMED last updated this device on Mar 19, 2026

K-Push

B-03770011995370

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: KINVENT Biomecanique
UDI-DI code: 03770011995370
Reference / catalog number: MP.05.02.FN

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Manufacturer information

Organization name: KINVENT Biomecanique
SRN: FR-MF-000031884
Manufacturer status: Active

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW010
Do not use on patients with Silver allergies.
CW020
The K-Push and accessories are provided non-sterile and are not compatible with autoclave or other sterilization techniques. Do not autoclave.

Market distribution

Primary placement in France; available across 1 country total.

Placed on the market in France; per-country availability dates not published.

Device identification

Trade name: K-Push
UDI-DI code: 03770011995370
Basic UDI-DI: B-03770011995370
Reference / catalog number: MP.05.02.FN
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: https://kinvent.com/kinvent-product/hand-held-dynamometer-k-push
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z120602PHYSIOTHERAPY EQUIPMENT

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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Certificates

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.