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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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Disposable powder-free latex… — 5 UDI-DI variants, MDR (CHEMIL Srl)

MD Atlas
CHEMIL Srl

Data from EUDAMED, last updated May 30, 2026

Disposable powder-free latex examination glove

80505935372191PFDCSU

5 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: CHEMIL Srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 80505935372191PFDCSU
Device name: Disposable powder-free latex examination glove
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 4, 2026

Manufacturer & authorised representative

Manufacturer

Name: CHEMIL Srl
SRN: IT-MF-000026789
Country: Italy
Email: info@chemil.com

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KQRZM8H837WRWVY6GE58KECD

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

72192PFDC18050593530834
72193PFDC18050593530841
72189PFDC18050593530803
72190PFDC18050593530810
72191PFDC18050593530827