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.

DT/01/DT/014 — 4 UDI-DI variants, MDR (C.O.C. FARMACEUTICI S.R.L.)

MD Atlas
C.O.C. FARMACEUTICI S.R.L.

Data from EUDAMED, last updated May 30, 2026

DT/01/DT/014

803395976DT01DT014ZJ

4 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: C.O.C. FARMACEUTICI 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: 803395976DT01DT014ZJ
Device name: —
Device model: DT/01/DT/014
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Nov 7, 2023

Manufacturer & authorised representative

Manufacturer

Name: C.O.C. FARMACEUTICI S.R.L.
SRN: IT-MF-000019321
Country: Italy
Email: info@contentgroup.it
Phone: +39 059 673911

Variants by status

UDI-DI variants

4 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

basicUdiUlid01HEMCXFRCKCJTKPQY2TSW19M8

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

DT/01/DT/01408033971601435
DT/01/DT/01408002945750325
DT/01/DT/01408008843008056
DT/01/DT/01405903060607040