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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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K-wire Ø2.4 L380 — 1 UDI-DI variant, MDD (Medacta International SA)

MD Atlas
Medacta International SA

Data from EUDAMED, last updated May 23, 2026

K-wire Ø2.4 L380

B-07630040716987

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIa

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: Medacta International SA

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Device characteristics

Reusable

Legacy certificates

Certificate number: MED 29022C
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: KIWA CERMET ITALIA S.P.A. (0476)
Validity: May 26, 2024

Identity & classification

Basic UDI-DI: B-07630040716987
Device name: K-wire Ø2.4 L380
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: Jan 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: Medacta International SA
SRN: CH-MF-000033473
Country: Switzerland
Email: info@medacta.ch
Phone: +41916966060

Authorised representative

Name: Medacta Italia srl
SRN: IT-AR-000022505
Country: Italy

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01GSZARASAX47AT1A3CW4GYDAZ

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

K-wire Ø2.4 L38007630040716987