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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

60213 — Class I MDR by Alegro Medical GmbH

MD Atlas
Alegro Medical GmbH

EUDAMED last updated this device on Apr 27, 2023

60213

PP00597ALGCFV00142

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Alegro Medical GmbH
UDI-DI code: 110364528155
Reference / catalog number: 60213

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Manufacturer information

Organization name: Alegro Medical GmbH
SRN: DE-MF-000026024
Manufacturer status: Active

Related devices

60211PP00597ALGCFV00142On the market 60212PP00597ALGCFV00142On the market 60007PP00597ALGCFV00142On the market 60005PP00597ALGCFV00142On the market 60002PP00597ALGCFV00142On the market

Critical warnings

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

CW129
Should not be used in phlebitis (septic phlebitis), deep vein thrombosis (phlegmasia coeruela dolens), in heart failure or over superinfected wounds. In case of ulcus cruris with arterial component, the valid rules must be observed.
CW133
Do not use in case of known allergy to phenoxyethano

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: 110364528155
Basic UDI-DI: PP00597ALGCFV00142
Reference / catalog number: 60213
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 5 m starr
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.