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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

AF go15 — Class I MDD by Look Ahead SRL

MD Atlas
Look Ahead SRL

EUDAMED last updated this device on Feb 5, 2024

AF go15

B-05940597842001

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Look Ahead SRL
UDI-DI code: 05940597842001
Reference / catalog number: AF go15

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View device family (Basic UDI)

Manufacturer information

Organization name: Look Ahead SRL
SRN: RO-MF-000001948
Manufacturer status: Active

Related devices

MSM g45, MSM g20B-MF-0000019486XOn the market MSFP cps10B-RO-MF-000001948HGOn the market PO g25, PO g45B-PO_gTEOn the market RS g15, RS g50, RS g100B-RS_gUGOn the market RS g15, RS g50, RS g100B-59405978420WDOn the market

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Romania; available across 1 country total.

Placed on the market in Romania; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 05940597842001
Basic UDI-DI: B-05940597842001
Reference / catalog number: AF go15
Issuing entity: GS1

Classification

Risk category: Class I
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: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

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

M9002PROTECTIVE DEVICES, LUBRICANTS AND SOOTHING DEVICES (SPRAYS, GELS, FLUIDS AND CREAMS)

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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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.