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.

Devices for percutaneous discectomy… — 205 UDI-DI variants, MDR

MD Atlas
Adria S.r.l.

Data from EUDAMED, last updated May 31, 2026

Devices for percutaneous discectomy and motorized for vertebroplasty / kyphoplasty

803373711K0299VX

205 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: Adria S.r.l.

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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 803373711K0299VX
Device name: Devices for percutaneous discectomy and motorized for vertebroplasty / kyphoplasty
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: Adria S.r.l.
SRN: IT-MF-000027852
Country: Italy
Email: customer-service@adriamedical.com
Phone: +39 0376 559772

Variants by status

UDI-DI variants

205 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

basicUdiUlid01KS7Y7W48A1GX73QKW6G4GVJ1

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

Spinertome kit08053175001671
Spinertome kit08053175001695
Spinertome kit08053175001626
Spinertome kit08053175001169
Spinertome kit08053175001084
Spinertome kit08053175001299
Spinertome kit08053175001428
Spinertome kit08053175001183
Spinertome kit08053175001220
Spinertome kit08053175001589
Spinertome kit08053175001688
Spinertome kit08053175001374
Spinertome kit08053175001008
Spinertome kit08053175001565
Spinertome kit08053175001268
Spinertome kit08053175001114
Spinertome kit08053175001725
Spinertome kit08053175001381
Spinertome kit08053175001596
Spinertome kit08053175001442
Spinertome kit08053175001060
Spinertome kit08053175001237
Spinertome kit08053175001510
Spinertome kit08053175000988
Spinertome kit08053175001138

3 4 5 6 7