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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

Vaginal Gel / Gel Vaginal 5 ml /… — Class IIb MDR

MD Atlas
Laboratorios Liconsa, S.A.

EUDAMED last updated this device on Jan 25, 2024

Vaginal Gel / Gel Vaginal 5 ml / 5 g

843604601VaginalGel5mlKP

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Laboratorios Liconsa, S.A.
UDI-DI code: 08436046010338
Reference / catalog number: Vaginal Gel / Gel Vaginal 5 ml / 5 g

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Manufacturer information

Organization name: Laboratorios Liconsa, S.A.
SRN: ES-MF-000009023
Manufacturer status: Active

Critical warnings

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

CW009
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW011
Tell your doctor or pharmacist if you are using, have recently used or might use any other barrier contraceptive method such as cervical caps, diaphragms, or contraceptive sponges with spermicide

Market distribution

Primary placement in Austria; available across 2 countries total.

Country	On market since	Until
AustriaPrimary placement		Still on market
Germany		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08436046010338
Basic UDI-DI: 843604601VaginalGel5mlKP
Reference / catalog number: Vaginal Gel / Gel Vaginal 5 ml / 5 g
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: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

A99DEVICES FOR ADMINISTRATION, WITHDRAWAL AND COLLECTION - 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

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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.