Organization name
UDI-DI code
Reference / catalog number

Manufacturer information

Organization name: JUST-ON
SRN: IT-MF-000044566
Manufacturer status: Active

Certificates

No certificates registered for this manufacturer.

Related devices

This device is not currently linked to any other device.

EUDAMED last updated this device on Feb 16, 2026

JO1

805559862JUST-ON6L

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: JUST-ON
UDI-DI code: 08055598620019
Reference / catalog number: JO1

View device family (Basic UDI)

Manufacturer information

Organization name: JUST-ON
SRN: IT-MF-000044566
Manufacturer status: Active

Critical warnings

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

CW999
Monouso
CW999
Non sterile
CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Italy; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 08055598620019
Basic UDI-DI: 805559862JUST-ON6L
Reference / catalog number: JO1
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: 20
Additional product description: Il dispositivo in oggetto è un dispositivo agganciabile, utilizzato per costituire un canale operativo applicabile a isteroscopi/cistoscopi diagnostici rigidi da 4 mm.
Additional information URL: https://www.juston.it/
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08055598620019

UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Z12020785GENITOURINARY ENDOSCOPY INSTRUMENTS - CONSUMABLES

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

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Related devices

This device is not currently linked to any other device.

Certificates

No certificates registered for this manufacturer.