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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 NON-SURGICAL NON-STERILE… — 5 UDI-DI variants, MDR

MD Atlas
Reflexx

Data from EUDAMED, last updated May 31, 2026

DISPOSABLE NON-SURGICAL NON-STERILE LATEX GLOVES WITH POWDER

803289163GLPPF2

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: Reflexx

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 803289163GLPPF2
Device name: DISPOSABLE NON-SURGICAL NON-STERILE LATEX GLOVES WITH POWDER
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: Reflexx
SRN: IT-MF-000021631
Country: Italy
Email: info@reflexx.com

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KMNCGGJ9JRABMPA8ENWSB279

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

REFLEXX 40 - SIZE L08032891631355
REFLEXX 40 - SIZE M08032891631348
REFLEXX 40 - SIZE S08032891631331
REFLEXX 40 - SIZE XL08032891631362
REFLEXX 40 - SIZE XS08032891631324