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.

PLIF SG Curette Rongeur — 23 UDI-DI variants, MDR

MD Atlas
Medos International SARL

Data from EUDAMED, last updated May 23, 2026

PLIF SG Curette Rongeur

0705034a000525P

23 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Medos International SARL

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

Reusable

Identity & classification

Basic UDI-DI: 0705034a000525P
Device name: PLIF SG Curette Rongeur
Device model: PLIF SG Bone Spoons and Curettes
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 15, 2025

Manufacturer & authorised representative

Manufacturer

Name: Medos International SARL
SRN: CH-MF-000014268
Country: Switzerland
Email: EUDAMED_Enquiries@its.jnj.com
Phone: +41 32 934 80 00

Authorised representative

Name: DePuy Ireland UC
SRN: IE-AR-000009328
Country: Ireland
Phone: +353 (0)21 4914000

Variants by status

UDI-DI variants

23 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

basicUdiUlid01K2QEVF9PYH7K6DAQJXQBMGWR

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

SPINAL INSTRUMENT10705034004334
SPINAL INSTRUMENT10705034008295
SPINAL INSTRUMENT10705034000169
SPINAL INSTRUMENT10705034000664
SPINAL INSTRUMENT10705034004372
SPINAL INSTRUMENT10705034000688
SPINAL INSTRUMENT10705034008288
SPINAL INSTRUMENT10705034000695
SPINAL INSTRUMENT10705034000671
SPINAL INSTRUMENT10705034000190
SPINAL INSTRUMENT10705034000183
SPINAL INSTRUMENT10705034000213
SPINAL INSTRUMENT10705034240565
SPINAL INSTRUMENT10705034236629
SPINAL INSTRUMENT10705034004358
SPINAL INSTRUMENT10705034000657
SPINAL INSTRUMENT10705034000152
SPINAL INSTRUMENT10705034184616
SPINAL INSTRUMENT10705034000718
SPINAL INSTRUMENT10705034004341
SPINAL INSTRUMENT10705034000732
SPINAL INSTRUMENT10705034000725
SPINAL INSTRUMENT10705034004327