Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Angled Blade Plate — 44 UDI-DI variants, MDR (Synthes GmbH)

MD Atlas
Synthes GmbH

Data from EUDAMED, last updated May 23, 2026

Angled Blade Plate

7611819a00467K4

44 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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 7611819a00467K4
Device name: Angled Blade Plate
Device model: Angled Blade Plate
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

UDI-DI variants

44 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01K1EEHVX3C3P1MG3BWGSQ9Q1R

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

238.94007611819007123
238.470S07611819262225
238.960S07611819262317
238.47007611819007048
238.490S07611819262249
238.940S07611819262300
238.49007611819007062
238.44007611819007017
238.360S07611819262140
238.66007611819007109
238.64007611819007093
238.420S07611819262188
238.680S07611819262294
238.600S07611819262256
238.68007611819007116
238.98007611819007147
238.42007611819007000
238.620S07611819262263
238.41007611819006997
238.440S07611819262195
238.260S07611819262126
238.60007611819007079
238.48007611819007055
238.410S07611819262171
238.40007611819006980

1 2