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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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Collant MICROFIBRA — 60 UDI-DI variants, MDR

MD Atlas
NEW MEDICAL SERVICE SRL

Data from EUDAMED, last updated May 31, 2026

Collant MICROFIBRA

80536857262480441P7

60 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: NEW MEDICAL SERVICE SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 80536857262480441P7
Device name: Collant MICROFIBRA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 8, 2025

Manufacturer & authorised representative

Manufacturer

Name: NEW MEDICAL SERVICE SRL
SRN: IT-MF-000034543
Country: Italy
Email: info@flebysan.it
Phone: +39425474993

Variants by status

UDI-DI variants

60 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K24A3SMJZE29CQ6DP786F0KF

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

805368572624808053685726248
805368572654508053685726545
805368572657608053685726576
805368572651408053685726514
805368572656908053685726569
805368572659008053685726590
805368572653808053685726538
805368572655208053685726552
805368572658308053685726583
805368572652108053685726521

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