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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

AQUADROP 2+ — Class IIb MDR by C.O.C. FARMACEUTICI…

MD Atlas
C.O.C. FARMACEUTICI S.R.L.

EUDAMED last updated this device on Feb 26, 2026

AQUADROP 2+

803395976DT01DT010ZA

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: C.O.C. FARMACEUTICI S.R.L.
UDI-DI code: 08057729510015
Reference / catalog number: DT/01/DT/010

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View device family (Basic UDI)

Manufacturer information

Organization name: C.O.C. FARMACEUTICI S.R.L.
SRN: IT-MF-000019321
Manufacturer status: Active

Related devices

DT/01/DT/002803395976DT01DT002ZBOn the market DT/01/DT/002803395976DT01DT002ZBOn the market DT/01/DT/002803395976DT01DT002ZBOn the market DT/01/DT/002803395976DT01DT002ZBOn the market DT/01/DT/003803395976DT01DT003ZDOn 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

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

CW262
The product is for single patient use [EN].
CW999
The product is for ophthalmic use only.
CW999
During application, do not touch the eye or any other surface with the container's dispensing edge.
CW999
Do not use in case of known incompatibility towards any of the components of the solution.
CW277
In case side effects during use, interrupt the treatment and consult a doctor [EN].
CW007
Do not use the product if the aluminum pouch is damaged or if the single dose is not perfectly closed [EN].
CW999
Keep out of the reach and sight of children.
CW275
Consult your doctor before you use this product if you are pregnant or breast-feeding [EN].
CW999
For external use, do not swallow.
CW036
No interactions with drugs or other eye drops are reported; however, leave at least 15 minutes between administrations of any other eye drops [EN].
CW999
Do not use if are visible particles and/or changes in the color of the solution.
CW032
Do not use after the expiry date indicated on the package and on the single dose [EN].
CW999
It is necessary to report any serious incident occurred in relation to the device to the manufacturer and the Competent authority of the Member state in which you are established.
CW999
Dispose of the product according to your local waste management regulations.

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Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: AQUADROP 2+
UDI-DI code: 08057729510015
Basic UDI-DI: 803395976DT01DT010ZA
Reference / catalog number: DT/01/DT/010
Issuing entity: GS1

Classification

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

Device details

Quantity: 30
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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