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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

40 — Class I MDR by Insausti Material…

MD Atlas
Insausti Material Clínico S.L.U.

EUDAMED last updated this device on Oct 28, 2021

40

8437022909ACC40VP

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Insausti Material Clínico S.L.U.
UDI-DI code: 18437022909063
Reference / catalog number: 40

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Manufacturer information

Organization name: Insausti Material Clínico S.L.U.
SRN: ES-MF-000003261
Manufacturer status: Active

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: 18437022909063
Basic UDI-DI: 8437022909ACC40VP
Reference / catalog number: 40
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: Serum holder
Additional information URL: https://www.insaustimedicaltrolleys.com/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V0880MEDICAL SUPPORT EQUIPMENT - ACCESSORIES

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

Related devices

MEDICAL TROLLEY8437022909TRODJOn the market 418437022909ACC41VROn the market 348437022909ACC34VUOn 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.