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

05435 — Class IIa MDD by Laboratorio Chimico…

MD Atlas
Laboratorio Chimico Farmaceutico A. Sella Srl

EUDAMED last updated this device on May 26, 2023

05435

B-08032632602019E8

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Laboratorio Chimico Farmaceutico A. Sella Srl
UDI-DI code: D-08032632602019E8
Reference / catalog number: 05435

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: Laboratorio Chimico Farmaceutico A. Sella Srl
SRN: IT-MF-000026481
Manufacturer status: Active

Related devices

02730B-08032632600930ETOn the market 3002601B-08032632601265EJOn the market 3001888B-08032632601302DXOn the market 3001742B-08032632601319EGOn the market 3704937B-8032632602415V2On 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.

Critical warnings

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

CW009
SYMBOL/ DISPOSITIVO MONOUSO/DISPOSABLE DEVICE
CW010
SYMBOL/LEGGERE ATTENTAMENTE IL FOGLIETTO ILLUSTRATIVO/READ THE LEAFLET
CW011
SYMBOL
CW135
TENERE FUORI DALLA PORTATA DEI BAMBINI/KEEP OUT OF THE REACH OF CHILDREN

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.

Country	On market since	Until
ItalyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: D-08032632602019E8
Basic UDI-DI: B-08032632602019E8
Reference / catalog number: 05435
Issuing entity: EUDAMED

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: 12 MICROENEMAS OF 9 G
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

D-08032632602019E8

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.

G99GASTROINTESTINAL DEVICES - OTHER

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