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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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Titanium Rod Ø 5.5mm — 62 UDI-DI variants, MDR (Synthes GmbH)

MD Atlas
Synthes GmbH

Data from EUDAMED, last updated May 23, 2026

Titanium Rod Ø 5.5mm

7611819a00402J8

62 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

62 UDI-DI variants

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Applied filters

basicUdiUlid01K25JFEFDCBG29TE5DDC6BY0Q

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

04.636.08007611819405554
04.636.05007611819401983
04.634.250S07611819539068
04.634.26007611819526044
04.634.25007611819526020
04.636.060S07611819470675
04.636.06507611819405516
04.634.255S07611819539075
04.636.06007611819405509
04.636.050S07611819470651
04.636.12507611819405578
04.634.29507611819526112
04.634.270S07611819539105
04.634.23507611819525993
04.634.28007611819526082
04.634.290S07611819539143
04.636.07007611819405523
04.636.08507611819405561
04.634.23007611819525986
04.634.29007611819526105
04.634.24007611819526006
04.633.290S07611819598126
04.634.32507611819526129
04.634.240S07611819539044
04.636.080S07611819470712

1 2 3

Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 7611819a00402J8
Device name: Titanium Rod Ø 5.5mm
Device model: Posterior Rods for Spine Titanium Rod Ø 5.5mm
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