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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

ENDO-RBC-SU — Class IIa MDR by Era Endoscopy Srl

MD Atlas
Era Endoscopy Srl

EUDAMED last updated this device on Jan 19, 2026

ENDO-RBC-SU

805361440SISENDOCOLON82

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Era Endoscopy Srl
UDI-DI code: 08053614400089
Reference / catalog number: ENDO-RBC-SU

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View device family (Basic UDI)

Manufacturer information

Organization name: Era Endoscopy Srl
SRN: IT-MF-000034111
Manufacturer status: Active

Critical warnings

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

CW018
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	Jan 19, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08053614400089
Basic UDI-DI: 805361440SISENDOCOLON82
Reference / catalog number: ENDO-RBC-SU
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
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)08053614400089

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UDI-PI DataMatrix

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

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EMDN nomenclature code(s)

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

Z12019007IRRIGATORS

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

ENDO-CSW805361440SISENDOCOLON82On the market ENDO-CSW-SU805361440SISENDOCOLON82On the market ENDO-WJT-SU805361440SISENDOCOLON82On the market ENDO-RBC805361440SISENDOCOLON82On the market EWSND-TC805361440SISENDOCOLON82On 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.