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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

309210200 — Class I MDD by Marianne Decker Haut-…

MD Atlas
Marianne Decker Haut- und Nagelzangenherstellung GmbH

EUDAMED last updated this device on May 17, 2024

309210200

B-04262464530127

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Marianne Decker Haut- und Nagelzangenherstellung GmbH
UDI-DI code: 04262464530127
Reference / catalog number: 309210200

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Manufacturer information

Organization name: Marianne Decker Haut- und Nagelzangenherstellung GmbH
SRN: DE-MF-000040458
Manufacturer status: Active

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3755120009-GERLB-04262464530356On the market 309212000B-04262464530257On the market 3754131009-GERLB-04262464530158On the market 309212600B-04262464530301On the market 309210300B-04262464530134On 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.

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: 04262464530127
Basic UDI-DI: B-04262464530127
Reference / catalog number: 309210200
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Headcutter 14cm, standard, box joined
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

L090999ORTHOPAEDIC SURGERY CUTTING INSTRUMENTS, REUSABLE - 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
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Software identification