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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

1-001, 1-002 — Class I MDD by ABINOX Piotr Szłapka

MD Atlas
ABINOX Piotr Szłapka

EUDAMED last updated this device on May 27, 2026

1-001, 1-002

B-59069357990170

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: ABINOX Piotr Szłapka
UDI-DI code: 59069357990170
Reference / catalog number: 1-001, 1-002

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Manufacturer information

Organization name: ABINOX Piotr Szłapka
SRN: PL-MF-000043281
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Poland; available across 1 country total.

Country	On market since	Until
PolandPrimary placement	Apr 16, 2014	Still on market

Device identification

Trade name: not provided
UDI-DI code: 59069357990170
Basic UDI-DI: B-59069357990170
Reference / catalog number: 1-001, 1-002
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: Stoliki do instrumentów chirurgicznych typu Mayo serii 1-001 i 1-002 przeznaczone są do odkładania instrumentów i narzędzi chirurgicznych lub urządzeń medycznych, podczas wykonywania badań i zabiegów medycznych na pacjencie w placówkach służby zdrowia.
Additional information URL: https://www.abinox.eu/
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

L99SURGICAL 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

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Related devices

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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.