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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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Rod Ø 6.0mm w/MIS Coupling — 61 UDI-DI variants, MDR (Synthes GmbH)

MD Atlas
Synthes GmbH

Data from EUDAMED, last updated May 23, 2026

Rod Ø 6.0mm w/MIS Coupling

7611819a00408JL

61 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

61 UDI-DI variants

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Applied filters

basicUdiUlid01K25JFEFFQKKV9XPJQ6FCZQAR

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

04.659.045S07611819598225
04.659.130S07611819598393
04.659.12007611819598904
04.659.230S07611819598478
04.659.08507611819598836
04.659.090S07611819598317
04.659.065S07611819598263
04.659.09507611819598850
04.659.290S07611819598492
04.659.140S07611819598409
04.659.200S07611819598461
04.659.125S07611819598386
04.659.170S07611819598430
04.659.06507611819598799
04.659.16007611819598959
04.659.20007611819598997
04.659.05507611819598775
04.659.040S07611819598218
04.659.07507611819598812
04.659.15007611819598942
04.659.110S07611819598355
04.659.11007611819598881
04.659.075S07611819598287
04.659.08007611819598829
04.659.12507611819598911

1 2 3

Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 7611819a00408JL
Device name: Rod Ø 6.0mm w/MIS Coupling
Device model: Posterior Rods for Spine Rod Ø 6.0mm w/MIS Coupling
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Aug 8, 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