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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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Vinyl Gloves — 5 UDI-DI variants, MDR (Berner Oy)

MD Atlas
Berner Oy

Data from EUDAMED, last updated May 23, 2026

Vinyl Gloves

641450BPVGH4

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: Berner Oy

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 641450BPVGH4
Device name: —
Device model: Vinyl Gloves
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 15, 2023

Manufacturer & authorised representative

Manufacturer

Name: Berner Oy
SRN: FI-MF-000007402
Country: Finland
Email: maria.liljelund@berner.fi

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01H7VT75Y7YCB9GJ5X97ZHF37N

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

BPVG100406414505177701
BPVG100306414505177688
BPVG100206414505177664
BPVG100506414505177725
BPVG100106414505188202