Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

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

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

Propriomed 2 — Class I MDR by HAIDER BIOSWING GmbH

MD Atlas
HAIDER BIOSWING GmbH

EUDAMED last updated this device on Oct 11, 2023

Propriomed 2

426074252BIO0044XA

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: HAIDER BIOSWING GmbH
UDI-DI code: 04260742520044
Reference / catalog number: Propriomed 2

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

Organization name: HAIDER BIOSWING GmbH
SRN: DE-MF-000008765
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Austria; available across 3 countries total.

Country	On market since	Until
AustriaPrimary placement		Still on market
Germany		Still on market
France		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260742520044
Basic UDI-DI: 426074252BIO0044XA
Reference / catalog number: Propriomed 2
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Sensomotorischer Schwingstab
Additional information URL: https://bioswing.de/wp-content/uploads/2022/01/Benutzerhandbuch-BIOSWING-Propriomed-MDR-2017.pdf
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z120603PASSIVE REHABILITATIVE GYMNASTICS 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

Related devices

Posturomed compact426074252BIO0020WUOn the market Posturomed 202426074252BIO0013WXOn the market Propriomed 1426074252BIO0037XDOn the market Propriomed 100426074252BIO0051X7On the market

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.