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.

USS Bone Screw Pedicle Screw Vertebral… — 412 UDI-DI variants, MDR

MD Atlas
Synthes GmbH

Data from EUDAMED, last updated May 23, 2026

USS Bone Screw Pedicle Screw Vertebral Body Screw Cancellous Low Profile Polyaxial Perforated Side-Opening

7611819a00269JW

412 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: 7611819a00269JW
Device name: USS Bone Screw Pedicle Screw Vertebral Body Screw Cancellous Low Profile Polyaxial Perforated Side-Opening
Device model: USS - Universal Spine System Bone Screw
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

UDI-DI variants

412 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

basicUdiUlid01K25JDS5T2EH85RSVKPJ8R1W6

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

499.201.75007611819156289
04.607.058S07611819950214
04.607.02107611819185593
04.607.257S07611819953123
04.607.02407611819185623
499.201.560S07611819966659
499.201.540S07611819966611
418.635S07611819966017
499.201.56507611819156111
418.837S07611819966130
04.607.05407611819185784
04.607.26107611819186156
499.26307611819815278
04.607.03707611819185739
04.607.272S07611819953239
04.607.033S07611819950085
04.607.059S07611819950221
418.62007611819144583
04.607.239S07611819952966
04.607.281S07611819953321
04.607.016S07611819949973
04.607.03407611819185708
418.825S07611819966093
499.201.770S07611819966840
499.201.675S07611819387478