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.

VOLT Small Fragment Plates… — 88 UDI-DI variants, MDR (Synthes GmbH)

MD Atlas
Synthes GmbH

Data from EUDAMED, last updated May 23, 2026

VOLT Small Fragment Plates Commercially Pure Titanium TiCP

7611819a00659KF

88 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: 7611819a00659KF
Device name: VOLT Small Fragment Plates Commercially Pure Titanium TiCP
Device model: VOLT Small Fragment Plates Commercially Pure Titanium TiCP
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 11, 2026

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

88 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

basicUdiUlid01KRC2P8SQPZ56YB72BK4PQSAH

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

04.535.00707612334248756
04.536.01007612334251954
04.535.05507612334248954
04.535.08807612334249296
04.535.084S07612334249227
04.536.012S07612334251985
04.535.05407612334248930
04.536.018S07612334252043
04.535.054S07612334248947
04.535.020S07612334248916
04.535.06207612334249074
04.535.06007612334249050
04.535.09007612334249319
04.535.057S07612334249005
04.535.014S07612334248862
04.535.086S07612334249265
04.536.036S07612334252135
04.535.062S07612334249081
04.536.020S07612334252050
04.535.00807612334248770
04.535.018S07612334248909
04.535.010S07612334248824
04.535.01407612334248855
04.535.08307612334249197
04.535.006S07612334248749

1 2 3 4