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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

IL710015 — Class III MDD by VIDA SRL

MD Atlas
VIDA SRL

EUDAMED last updated this device on Jun 13, 2025

IL710015

B-INFINIPREMIUMFILLERUK

On the marketClass III

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: VIDA SRL
UDI-DI code: D-INFINIPREMIUMFILLERUK
Reference / catalog number: IL710015

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View device family (Basic UDI)

Manufacturer information

Organization name: VIDA SRL
SRN: IT-MF-000030547
Manufacturer status: Active

Critical warnings

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

CW011
EUDAMED did not publish a description for this code.
CW010
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.
CW032
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	Mar 30, 2021	Still on market

Device identification

Trade name: not provided
UDI-DI code: D-INFINIPREMIUMFILLERUK
Basic UDI-DI: B-INFINIPREMIUMFILLERUK
Reference / catalog number: IL710015
Issuing entity: EUDAMED

Classification

Risk category: Class III
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: 1X1ml

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

D-INFINIPREMIUMFILLERUK

DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

P900402RESORBABLE FILLING AND RECONSTRUCTION DEVICES

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

IL710176B-INFINIPREMIUMFILLERAK6On the market IL710145B-INFINIPREMIUMFILLERSLFLOn the market IL710107B-INFINIPREMIUMFILLERBK8On the market IL710022B-INFINIPREMIUMFILLERMKWOn the market IL710039B-INFINIPREMIUMFILLERSLAOn the market

Certificates

Certificate health across this manufacturer's portfolio.

CSQ003626Issued
Quality management systemNotified body: 0373Expiry: Apr 9, 2031