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Organization name
UDI-DI code
Reference / catalog number

Golamir Tablets to be dissolved… — Class IIa MDR

MD Atlas
ABOCA S.P.A. SOCIETÀ AGRICOLA

EUDAMED last updated this device on Mar 7, 2025

Golamir Tablets to be dissolved in the mouth

8032472GOL2ax1V8

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ABOCA S.P.A. SOCIETÀ AGRICOLA
UDI-DI code: 08032472029779
Reference / catalog number: 08032472029779

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View device family (Basic UDI)

Manufacturer information

Organization name: ABOCA S.P.A. SOCIETÀ AGRICOLA
SRN: IT-MF-000029499
Manufacturer status: Active

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Certificates

Certificate health across this manufacturer's portfolio.

CVD002223Issued
Technical documentationNotified body: 0373Expiry: Mar 26, 2028
CSQ0009230223Supplemented
Quality management systemNotified body: 0373Expiry: Mar 26, 2028

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Cyprus; available across 3 countries total.

Country	On market since	Until
CyprusPrimary placement		Still on market
EL		Still on market
Malta		Still on market

Device identification

Trade name: Golamir Tablets to be dissolved in the mouth
UDI-DI code: 08032472029779
Basic UDI-DI: 8032472GOL2ax1V8
Reference / catalog number: 08032472029779
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 2
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08032472029779

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

V9017ORAL ADMINISTRATION PREPARATIONS NOT INCLUDED IN OTHER CLASSES

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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