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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

SC8011800000004 — Class I MDR by INDUSTRIAS HIDRÁULICAS…

MD Atlas
INDUSTRIAS HIDRÁULICAS PARDO SL

EUDAMED last updated this device on Aug 8, 2023

SC8011800000004

8431212TECHNOPLUS-ICU-UF

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: INDUSTRIAS HIDRÁULICAS PARDO SL
UDI-DI code: 08431212240908
Reference / catalog number: SC8011800000004

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Manufacturer information

Organization name: INDUSTRIAS HIDRÁULICAS PARDO SL
SRN: ES-MF-000015121
Manufacturer status: Active

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SC80194000000088431212ADVANTMEOn the market SG80122000000718431212GERIATRICA-BORA5POn the market SC80181000000058431212NEWCARE-V1-7YOn the market SC80181000000278431212NEWCARE-V1-7YOn the market SC80140000000038431212ATICAR2On 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 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: 08431212240908
Basic UDI-DI: 8431212TECHNOPLUS-ICU-UF
Reference / catalog number: SC8011800000004
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V08060101HOSPITAL/HOME CARE ELECTRIC MEDICAL BEDS

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
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Software identification