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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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DT/01/DT/005 — 11 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/005

803395976DT01DT005ZH

11 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.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 803395976DT01DT005ZH
Device name: —
Device model: DT/01/DT/005
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Mar 31, 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

11 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GWV6ZKTRSBVT802H605PS2GM

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/00508595566420895
DT/01/DT/00508595566423407
DT/01/DT00508033959761120
DT/01/DT/00508033959760260
DT/01/DT00508436561331284
DT/01/DT/00508033959761052
DT/01/DT/00508033661808052
DT/01/DT/00508033959760673
DT/01/DT/00508056149140314
DT/01/DT/00508033959760154
DT/01/DT/00503858882102735