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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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C_SP — 32 UDI-DI variants, MDR (PLURITEX SRL)

MD Atlas
PLURITEX SRL

Data from EUDAMED, last updated May 30, 2026

C_SP

805938667C_SPQW

32 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: PLURITEX SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805938667C_SPQW
Device name: C_SP
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 28, 2022

Manufacturer & authorised representative

Manufacturer

Name: PLURITEX SRL
SRN: IT-MF-000024111
Country: Italy
Email: info@pluritex.it
Phone: +39 0 524 533417

Variants by status

UDI-DI variants

32 UDI-DI variants

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Applied filters

basicUdiUlid01G6NEYH0S67PVCCF19ERM92GS

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

1HE4D - TG.S08059386671016
1HE4D - TG. XL08059386671047
FB21 - TG. L08059386671580
FB24 - TG. XL08059386671597
9TC01 TG. 2XL08059386672389
9TC01 TG.L08059386672372
9TC01 TG.M08059386672365

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