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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

71026 — Class I MDR by Most Active Health Care…

MD Atlas
Most Active Health Care GmbH

EUDAMED last updated this device on Sep 23, 2022

71026

PP01576MAHCFV000501

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Most Active Health Care GmbH
UDI-DI code: 111421126164
Reference / catalog number: 71026

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Manufacturer information

Organization name: Most Active Health Care GmbH
SRN: DE-MF-000013735
Manufacturer status: Inactive

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Critical warnings

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

CW129
Not for peripheral arterial occlusive diseases, phlebitis (septic phlebitis), deep vein thrombosis (phlegmasia coeruela dolens ), in heart failure or over superinfected wounds. Do not use in case of known allergy to phenoxyethanol.
CW133
Do not use in case of known allergy to phenoxyethanol.

Market distribution

Primary placement in Germany; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 111421126164
Basic UDI-DI: PP01576MAHCFV000501
Reference / catalog number: 71026
Issuing entity: IFA

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 10
Additional product description: 10 cm x 10 m
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M03020299MEDICATED BANDAGES, WITH ZINC OXIDE AND OTHER COMPONENTS - OTHER

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.