Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners 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

RL301REVELLO — Class I MDR by Dispotech srl

MD Atlas
Dispotech srl

EUDAMED last updated this device on Mar 23, 2026

RL301REVELLO

++G066RL30N2W

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Dispotech srl
UDI-DI code: G066RL301REVELLO2
Reference / catalog number: RL301REVELLO

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?

View device family (Basic UDI)

Manufacturer information

Organization name: Dispotech srl
SRN: IT-MF-000010735
Manufacturer status: Active

Certificates

Certificate health across this manufacturer's portfolio.

ITD 1344523 1Supplemented
Quality assuranceNotified body: 1936Expiry: Jul 29, 2029

Critical warnings

No critical warnings reported for this device.

EasyUDICompliance engine

Sponsored

Your devices, UDI-compliant — without drowning in regulation

EUDAMED-ready· UDI-enriched

Basic UDIUDI-DIUDI-PIAttributeDocument

Print-ready label

From your product file — no manual entry

Exclusive to MD Atlas usersClaim my −20% discount

by Made In Tracker

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: G066RL301REVELLO2
Basic UDI-DI: ++G066RL30N2W
Reference / catalog number: RL301REVELLO
Issuing entity: HIBCC

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: —
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

G066RL301REVELLO2

DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.

EMDN nomenclature code(s)

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

Q019004DENTAL COTTON ROLLS

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

Become a partner of MD Atlas

Related devices

SF1853PROCLI++G066SFDIS6ZOn the market SF1853OMNIDENT24++G066SFDIS6ZOn the market SF1854DITEK++G066SFDIS6ZOn the market SF1854COSWELL2++G066SFDIS6ZOn the market SF1853COSWELL24++G066SFDIS6ZOn the market