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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

703-010 — Class III MDD by Kuros Biosciences

MD Atlas
Kuros Biosciences

EUDAMED last updated this device on Mar 10, 2026

703-010

B-08719699710559

On the marketClass III

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Kuros Biosciences
UDI-DI code: 08719699710559
Reference / catalog number: 703-010

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View device family (Basic UDI)

Manufacturer information

Organization name: Kuros Biosciences
SRN: NL-MF-000010905
Manufacturer status: Active

Related devices

703-038B-08719699710900On the market 703-035B-08719699710870On the market 703-043B-08719699710849On the market 703-029B-08719699710771On the market 703-016B-08719699710610On the market

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Netherlands; available across 1 country total.

Country	On market since	Until
NetherlandsPrimary placement	Sep 19, 2019	Mar 17, 2020

Device identification

Trade name: not provided
UDI-DI code: 08719699710559
Basic UDI-DI: B-08719699710559
Reference / catalog number: 703-010
Issuing entity: GS1

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: Synthetic Bone Void Filler
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 2 MU12

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08719699710559

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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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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.