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.

VIPER Spine System Straight Rods… — 129 UDI-DI variants, MDR

MD Atlas
Medos International SARL

Data from EUDAMED, last updated May 23, 2026

VIPER Spine System Straight Rods Straight Rod, Pre-Bent Rod, Pre-Kyphosed, Pre-Lordosed

0705034a002105H

129 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: 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

Implantable

Identity & classification

Basic UDI-DI: 0705034a002105H
Device name: VIPER Spine System Straight Rods Straight Rod, Pre-Bent Rod, Pre-Kyphosed, Pre-Lordosed
Device model: VIPER Spine System Rods
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Mar 18, 2026

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

129 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

basicUdiUlid01KM0WRRZBXD7MSC84FYNC21NP

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

VIPER2 SYSTEM10705034131788
VIPER2 SYSTEM10705034131832
VIPER2 SYSTEM10705034131894
VIPER2 SYSTEM10705034130903
VIPER2 SYSTEM10705034131795
VIPER2 SYSTEM10705034131818
VIPER2 SYSTEM10705034133522
VIPER2 SYSTEM10705034131726
VIPER2 SYSTEM10705034132860
VIPER2 SYSTEM10705034131740
VIPER2 SYSTEM10705034130880
VIPER2 SYSTEM10705034133362
VIPER2 SYSTEM10705034132907
VIPER2 SYSTEM10705034133164
VIPER2 SYSTEM10705034132808
VIPER2 SYSTEM10705034131757
VIPER2 SYSTEM10705034131047
VIPER2 SYSTEM10705034132051
VIPER2 SYSTEM10705034130811
VIPER2 SYSTEM10705034130866
VIPER2 SYSTEM10705034130941
VIPER2 SYSTEM10705034132662
VIPER2 SYSTEM10705034132648
VIPER2 SYSTEM10705034132921
VIPER2 SYSTEM10705034131825

2 3 4 5 6