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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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Safety IV Catheters with closed system — 119 UDI-DI variants, MDR

MD Atlas
Delta Med SPA

Data from EUDAMED, last updated May 30, 2026

Safety IV Catheters with closed system

80322485100089

119 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: Delta Med SPA

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UDI-DI variants

119 UDI-DI variants

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Applied filters

basicUdiUlid01JZT69WSN3ZD9D3G32G8031ZE

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

B-BLOCK.PRO G18X25 PUR R08032248512672
B-BLOCK.PRO G18X25 PUR RNL08032248512788
B-BLOCK.PRO G18X32 PUR R08032248512689
B-BLOCK.PRO G18X32 PUR RNL08032248512795
B-BLOCK.PRO G18X45 PUR R08032248512696
B-BLOCK.PRO G18X45 PUR RNL08032248512801
B-BLOCK.PRO G20X25 PUR R08032248512641
B-BLOCK.PRO G20X25 PUR RNL08032248512757
B-BLOCK.PRO G20X32 PUR R08032248512658
B-BLOCK.PRO G20X32 PUR RNL08032248512764
B-BLOCK.PRO G20X45 PUR R08032248512665
B-BLOCK.PRO G20X45 PUR RNL08032248512771
B-BLOCK.PRO G22X19 PUR R08032248512627
B-BLOCK.PRO G22X19 PUR RNL08032248512733
B-BLOCK.PRO G22X25 PUR R08032248512634
B-BLOCK.PRO G22X25 PUR RNL08032248512740
B-BLOCK.PRO G24X19 PUR R08032248512610
B-BLOCK.PRO G24X19 PUR RNL08032248512726
B-BLOCK.PRO G26X19 PUR R08032248512603
B-BLOCK.PRO Y G18X25 PUR PLL08032248512894
B-BLOCK.PRO Y G18X25 PUR PNL08032248513006
B-BLOCK.PRO Y G18X32 PUR PLL08032248512900
B-BLOCK.PRO Y G18X32 PUR PNL08032248513013
B-BLOCK.PRO Y G18X45 PUR PLL08032248512917
B-BLOCK.PRO Y G18X45 PUR PNL08032248513020

1 2 3 4 5

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 80322485100089
Device name: —
Device model: Safety IV Catheters with closed system
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jul 11, 2025

Manufacturer & authorised representative

Manufacturer

Name: Delta Med SPA
SRN: IT-MF-000027962
Country: Italy
Email: info@numantec.eu

Variants by status