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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

ReDura — Class III MDD by Medprin Biotech GmbH

MD Atlas
Medprin Biotech GmbH

EUDAMED last updated this device on Sep 5, 2022

ReDura

B-04260333310085

On the marketClass III

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Medprin Biotech GmbH
UDI-DI code: 04260333310085
Reference / catalog number: RDS-8

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Manufacturer information

Organization name: Medprin Biotech GmbH
SRN: DE-MF-000012291
Manufacturer status: Active

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NeoDuraB-04260333310221On the market NeoDuraB-04260333310290On the market NeoDuraB-04260333310238On the market NeoDuraB-04260333310252On the market NeoDuraB-04260333310337On the market

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Feb 12, 2016	Still on market

Device identification

Trade name: ReDura
UDI-DI code: 04260333310085
Basic UDI-DI: B-04260333310085
Reference / catalog number: RDS-8
Issuing entity: GS1

Classification

Risk category: Class III
Applicable legislation: MDD [Directive 93/42/EEC 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)

P900399TISSUE PATCHES - 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.