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

DBC MB Multipirpose Bench — Class I MDR by DBC Global Oy

MD Atlas
DBC Global Oy

EUDAMED last updated this device on Nov 17, 2022

DBC MB Multipirpose Bench

64298109805620WZ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: DBC Global Oy
UDI-DI code: 06429810980106
Reference / catalog number: DBC MB 5620

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: DBC Global Oy
SRN: FI-MF-000024338
Manufacturer status: Active

Market distribution

Primary placement in Finland; available across 1 country total.

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

Device identification

Trade name: DBC MB Multipirpose Bench
UDI-DI code: 06429810980106
Basic UDI-DI: 64298109805620WZ
Reference / catalog number: DBC MB 5620
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: Multipurpose Bench rehabilitation/exercise device
Additional information URL: https://www.dbc.fi/dbc-services
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

Related devices

DBC C3R Cervical 3D Rotation64298109805220WDOn the market DBC CE Cervical Extension64298109806160WTOn the market DBC GHR Glenohumeral Rotation64298109805420WPOn the market DBC Health64298109806429810980991B9On the market DBC LTE Lumbar Thoracic Extension64298109806110WCOn 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.