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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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VA LCP Dorsal Distal Radius Plate… — 40 UDI-DI variants, MDR

MD Atlas
Synthes GmbH

Data from EUDAMED, last updated May 23, 2026

VA LCP Dorsal Distal Radius Plate 2.4mm TICP

7611819a00371JN

40 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Synthes GmbH

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UDI-DI variants

40 UDI-DI variants

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basicUdiUlid01K1EEHPCZ81VR8JAPV7PWP59E

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

04.115.451S07611819461338
04.115.45007611819433380
04.115.23107611819422926
04.115.530S07611819461345
04.115.430S07611819461307
04.115.45107611819433397
04.115.350S07611819461291
04.115.15107611819433342
04.115.641S07611819461390
04.115.64107611819428270
04.115.151S07611819461239
04.115.251S07611819461277
04.115.450S07611819461321
04.115.231S07611819461253
04.115.131S07611819461215
04.115.631S07611819461376
04.115.150S07611819461222
04.115.431S07611819461314
04.115.640S07611819461383
04.115.13107611819422889
04.115.250S07611819461260
04.115.33007611819422957
04.115.130S07611819461208
04.115.63107611819428256
04.115.53007611819423015

1 2

Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 7611819a00371JN
Device name: VA LCP Dorsal Distal Radius Plate 2.4mm TICP
Device model: VA LCP Dorsal Distal Radius Plate 2.4mm TICP
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jul 30, 2025

Manufacturer & authorised representative

Manufacturer

Name: Synthes GmbH
SRN: CH-MF-000013345
Country: Switzerland
Email: EUDAMED_Enquiries@its.jnj.com
Phone: +41 (0) 61 965 61 11

Authorised representative

Name: DePuy Ireland UC
SRN: IE-AR-000009328
Country: Ireland
Phone: +353 (0)21 4914000

Variants by status