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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

VERSOL® sterile sodium chloride… — Class IIa MDD

MD Atlas
Laboratoire Aguettant

EUDAMED last updated this device on Apr 2, 2026

VERSOL® sterile sodium chloride 0.9% 1000mL

B-FR-MF-000000509600020RN

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Laboratoire Aguettant
UDI-DI code: D-FR-MF-000000509600020RN
Reference / catalog number: 600020

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Manufacturer information

Organization name: Laboratoire Aguettant
SRN: FR-MF-000000509
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.
CW007
EUDAMED did not publish a description for this code.
CW999
Do not inject.

Market distribution

Primary placement in France; available across 2 countries total.

Country	On market since	Until
FrancePrimary placement		Still on market
Malta		Still on market

Device identification

Trade name: VERSOL® sterile sodium chloride 0.9% 1000mL
UDI-DI code: D-FR-MF-000000509600020RN
Basic UDI-DI: B-FR-MF-000000509600020RN
Reference / catalog number: 600020
Issuing entity: EUDAMED

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: VERSOL® sterile sodium chloride 0.9% is indicated pre, per and post-operatively for: - Cleaning wounds, - Irrigation of wounds or dressings.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V0999FLUIDS/GASES FOR CLINICAL/THERAPEUTICAL USE - 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.