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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

AKL — Class I MDD by ROKO SP. Z O.O.

MD Atlas
ROKO SP. Z O.O.

EUDAMED last updated this device on Nov 25, 2025

AKL

B-05901421260057

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: ROKO SP. Z O.O.
UDI-DI code: 05901421260057
Reference / catalog number: AKL

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Manufacturer information

Organization name: ROKO SP. Z O.O.
SRN: PL-MF-000050171
Manufacturer status: Active

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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	Sep 15, 2011	Still on market

Device identification

Trade name: not provided
UDI-DI code: 05901421260057
Basic UDI-DI: B-05901421260057
Reference / catalog number: AKL
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: ACRON is dedicated for the production of partial denture plates – sedentary and partially supported, retention elements in metal skeletal dentures, microdentures, space retainers. The material is intended for the production of dental dentures using the pressure injection method only. ACRON's ideal chemical purity makes it a fully biocompatible material. Its neutral effect on the patient's health is confirmed by the certificates of the National Institute of Medicines.
Additional information URL: https://rokodent.pl/termoplasty/
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.

Q010699MATERIALS FOR THE PREPARATION OF CUSTOM-MADE DENTAL DEVICES - 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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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.