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

AN1053010 — Class I MDR by Creo Medical, S.L.U.

MD Atlas
Creo Medical, S.L.U.

EUDAMED last updated this device on Nov 11, 2024

AN1053010

843603713GH.020W7

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Creo Medical, S.L.U.
UDI-DI code: 08436037135705
Reference / catalog number: AN1053010

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: Creo Medical, S.L.U.
SRN: ES-MF-000000385
Manufacturer status: Active

Related devices

AN1066523843603713GH.020W7On the market AN2533010843603713GH.020W7On the market AN1053007843603713GH.020W7On the market AN2530110843603713GH.020W7On the market AN1866523843603713GH.020W7On 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.

Market distribution

Primary placement in France; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 08436037135705
Basic UDI-DI: 843603713GH.020W7
Reference / catalog number: AN1053010
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: ScopeClean - cepillo de limpieza, cepillo individual de 3 mm, vaina Ø 1,6 mm, longitud 100 cm
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V070101ENDOSCOPES CLEANING BRUSHES - FOR GENERIC USE

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