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

04.607.05807611819185821
04.607.01507611819185579
04.607.02907611819185678
04.607.034S07611819950092
04.607.46907611819801301
04.607.280S07611819953314
04.607.014S07611819949959
04.607.25207611819186064
04.607.23907611819185999
499.201.660S07611819966734
04.607.274S07611819953253
04.607.03207611819185685
04.607.467S07611819953543
499.260S07611819966949
04.607.05607611819185807
04.607.28007611819186286
04.607.02607611819185647
04.607.039S07611819950146
04.607.289S07611819953383
04.607.27707611819186255
499.201.775S07611819966857
499.264S07611819966987
04.607.012S07611819949935
04.607.25807611819186125
04.607.013S07611819949942

2 3 4 5 6