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UDI-DI code
Reference / catalog number

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Organization name
UDI-DI code
Reference / catalog number

Sterile Dropper — Class I MDR by Dompé farmaceutici s.p.a.

MD Atlas
Dompé farmaceutici s.p.a.

Manufacturer information

Organization name: Dompé farmaceutici s.p.a.
SRN: IT-MF-000016097
Manufacturer status: Active

Certificates

Certificate health across this manufacturer's portfolio.

ITD 1343612 1Supplemented
Quality assuranceNotified body: 1936Expiry: Oct 22, 2029

Related devices

Pipette802482500006DMMMOn the market

EUDAMED last updated this device on Oct 6, 2025

Sterile Dropper

802482500007DMMS

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Dompé farmaceutici s.p.a.
UDI-DI code: 08024825001860
Reference / catalog number: SI.06

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View device family (Basic UDI)

Manufacturer information

Organization name: Dompé farmaceutici s.p.a.
SRN: IT-MF-000016097
Manufacturer status: Active

Related devices

Pipette802482500006DMMMOn the market

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW009
EUDAMED did not publish a description for this code.
CW001
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Italy; available across 1 country total.

Placed on the market in Italy; per-country availability dates not published.

Device identification

Trade name: Sterile Dropper
UDI-DI code: 08024825001860
Basic UDI-DI: 802482500007DMMS
Reference / catalog number: SI.06
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: —
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

EMDN nomenclature code(s)

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

Q0299OPHTHALMIC 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

Certificate health across this manufacturer's portfolio.

ITD 1343612 1Supplemented
Quality assuranceNotified body: 1936Expiry: Oct 22, 2029