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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

PLANFERTIL GEL — Class IIb MDR by Crab Sinergy Srl

MD Atlas
Crab Sinergy Srl

EUDAMED last updated this device on Oct 17, 2025

PLANFERTIL GEL

8033776702287001J3

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Crab Sinergy Srl
UDI-DI code: 08033776700869
Reference / catalog number: PLF G 001

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View device family (Basic UDI)

Manufacturer information

Organization name: Crab Sinergy Srl
SRN: IT-MF-000008825
Manufacturer status: Active

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.
CW135
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement		Still on market

Device identification

Trade name: PLANFERTIL GEL
UDI-DI code: 08033776700869
Basic UDI-DI: 8033776702287001J3
Reference / catalog number: PLF G 001
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: LUBRICANT VAGINAL GEL FOR VAGINAL DRYNESS. IT HELPS TO MANTAIN THE PHYSIOLOGICAL WELL-BEING OF VAGINAL MUCUS AND SPERM
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)08033776700869

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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.

U0803VAGINAL DEVICES IN THE FORM OF SOLUTIONS/CREAMS/OVA/TABLETS

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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Related devices

BNIS001803377670192350MAOn the market AR1354803377670192350MAOn the market AR1359803377670192350MAOn the market VHG005 IT8033776702287001J3On the market HYALSOLO GEL8033776702287001J3On 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.