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

CH-2135-APR — Class I MDR by MOBERCAS SL

MD Atlas
MOBERCAS SL

EUDAMED last updated this device on Jul 19, 2023

CH-2135-APR

843659137CH-2135-APR42

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MOBERCAS SL
UDI-DI code: 08436591371502
Reference / catalog number: CH-2135-APR

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: MOBERCAS SL
SRN: ES-MF-000025078
Manufacturer status: Active

Related devices

CDF-10843659137CDF-1092On the market CDF-20843659137CDF-2095On the market CDF-25843659137CDF-259FOn the market CDF-30-PC843659137CDF-30-PCN8On the market CDF-BOBATH-10843659137CDF-BOBATH-10TGOn the market

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: 08436591371502
Basic UDI-DI: 843659137CH-2135-APR42
Reference / catalog number: CH-2135-APR
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: Hydraulic couch of 3 sections with individual leg sections and wheels.
Additional information URL: https://www.mobercas.com/ifu
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V08050101GENERIC USE STRETCHERS

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

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.