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.

Surgical instruments — 133 UDI-DI variants, MDR (ZIACOM ITS S.r.l.)

MD Atlas
ZIACOM ITS S.r.l.

Data from EUDAMED, last updated May 30, 2026

Surgical instruments

805957100STRUMENTARIO9V

133 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: ZIACOM ITS 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

Reusable

Identity & classification

Basic UDI-DI: 805957100STRUMENTARIO9V
Device name: Surgical instruments
Device model: Surgical instruments
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: ZIACOM ITS S.r.l.
SRN: IT-MF-000028897
Country: Italy
Email: formazione@itsitaly.it
Phone: +39 049 8642417

Variants by status

UDI-DI variants

133 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

basicUdiUlid01KSHMHKMX10CBBDZ5BF8QK61K

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

DR 812108059571001338
REI-0408059571006227
DR 811408059571241307
CD 711008059571000362
DR 813708059571001468
DR 813608059571001451
DR 818308059571001659
DR 814608059571001529
DRC 830008059571001925
HDS 740208059571002786
DR 812508059571001369
DS 730108059571001994
DR 810408059571171239
CD 732208059571000430
DR 812408059571001352
CD 711108059571000379
CLT 008059571007101
CD 713008059571000409
DRA 861008059571001789
DR 813308059571001437
STP 51108059571006524
DRC 830108059571001932
STP 51008059571006517
DRA 830008059571001680
DR 810408059571001239

1 2 3 4 5