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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

990500 FR — Class I MDR by novacare gmbh

MD Atlas
novacare gmbh

EUDAMED last updated this device on Apr 4, 2022

990500 FR

42504796V0807012M

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: novacare gmbh
UDI-DI code: 04250479615359
Reference / catalog number: 990500 FR

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Manufacturer information

Organization name: novacare gmbh
SRN: DE-MF-000007623
Manufacturer status: Active

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98210942504796Y12210327On the market 98211042504796Y12210327On the market 99400242504796V0807022POn the market 99420242504796V0811BROn the market 10185242504796V0807012MOn 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

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

CW011
Alternating pressure systems do not replace the regular, manual change of position of the patient by the nursing staff.
CW030
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW137
EUDAMED did not publish a description for this code.
CW138
EUDAMED did not publish a description for this code.

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: 04250479615359
Basic UDI-DI: 42504796V0807012M
Reference / catalog number: 990500 FR
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)

V080701ACTIVE ANTI-DECUBITUS MEDICAL MATTRESSES

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