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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

78054 — Class I MDR by Deluxe Medicrafts srl

MD Atlas
Deluxe Medicrafts srl

EUDAMED last updated this device on May 19, 2026

78054

5949556868VATAMEDZIGQG

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Deluxe Medicrafts srl
UDI-DI code: 05949556868106
Reference / catalog number: 78054

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View device family (Basic UDI)

Manufacturer information

Organization name: Deluxe Medicrafts srl
SRN: RO-MF-000050851
Manufacturer status: Active

Related devices

89060124622515949556868FESITIFONB120UMOn the market 89060124622525949556868FESITIFONB120UMOn the market 780555949556868VATAMEDZIGQGOn the market 89060124622505949556868FESITIFONB120UMOn the market CFXL5949556868COSTUMMEDICALLWOn 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.

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Romania; available across 1 country total.

Country	On market since	Until
RomaniaPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 05949556868106
Basic UDI-DI: 5949556868VATAMEDZIGQG
Reference / catalog number: 78054
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: VATA MEDICINALA DIN BUMBAC 200 gr
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)05949556868106

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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.

M010101HYDROPHILIC COTTON

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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