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Organization name
UDI-DI code
Reference / catalog number

2F MESH Lichtenstein PET3D — Class IIb MDD by MICROVAL

MD Atlas
MICROVAL

EUDAMED last updated this device on Apr 15, 2026

2F MESH Lichtenstein PET3D

B-03700458404203

On the marketClass IIb

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: MICROVAL
UDI-DI code: 03700458404203
Reference / catalog number: DS666117

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Manufacturer information

Organization name: MICROVAL
SRN: FR-MF-000003450
Manufacturer status: Active

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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.

Critical warnings

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

CW001
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW018
EUDAMED did not publish a description for this code.

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: 2F MESH Lichtenstein PET3D
UDI-DI code: 03700458404203
Basic UDI-DI: B-03700458404203
Reference / catalog number: DS666117
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDD [Directive 93/42/EEC 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: 7x10 cm

EMDN nomenclature code(s)

P900205POLYESTER SURGICAL MESHES

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