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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

996500 UK — Class I MDR by novacare gmbh

MD Atlas
novacare gmbh

EUDAMED last updated this device on Mar 31, 2022

996500 UK

42504796V0807012M

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: novacare gmbh
UDI-DI code: 04250479620292
Reference / catalog number: 996500 UK

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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
Caution – 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 XI; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 04250479620292
Basic UDI-DI: 42504796V0807012M
Reference / catalog number: 996500 UK
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