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

3101030 — Class I MDR by Fleming Comercial, S.A.

MD Atlas
Fleming Comercial, S.A.

EUDAMED last updated this device on Oct 13, 2022

3101030

8426828uriconDY

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Fleming Comercial, S.A.
UDI-DI code: 08470004716078
Reference / catalog number: 3101030

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: Fleming Comercial, S.A.
SRN: ES-MF-000004259
Manufacturer status: Active

Related devices

31050108426828bragacerradaLCOn the market 31050128426828bragacerradaLCOn the market 31050048426828bragacerradaLCOn the market 31050068426828bragacerradaLCOn the market 31050088426828bragacerradaLCOn 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

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

CW009
Once it is removed it can no longer be used
CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Spain; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 08470004716078
Basic UDI-DI: 8426828uriconDY
Reference / catalog number: 3101030
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: Diámetro 30mm / Contiene 30uds / C.N. 471607.8
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 30 MU50
159–173 MU50

EMDN nomenclature code(s)

U070299EXTERNAL DEVICES FOR THE TREATMENT OF INCONTINENCE - 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification