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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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THD Opti-Fiber — 3 UDI-DI variants, MDR (THD S.P.A.)

MD Atlas
THD S.P.A.

Data from EUDAMED, last updated May 30, 2026

THD Opti-Fiber

803373771FOC000176

3 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: THD S.P.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 803373771FOC000176
Device name: THD Opti-Fiber
Device model: THD Opti-Fiber
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 3, 2023

Manufacturer & authorised representative

Manufacturer

Name: THD S.P.A.
SRN: IT-MF-000029427
Country: Italy
Email: regulatory@thdlab.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01H4E2J6DZ2RD8W4ZNBBTFHA13

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

88001808033737710784
88000218033737710804
88001208033737710777