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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 Examination and Protective… — 10 UDI-DI variants, MDR

MD Atlas
Granberg AS

Data from EUDAMED, last updated May 30, 2026

Disposable Examination and Protective Nitrile Gloves Granberg®

702377GR114NHNSRS

10 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: Granberg AS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 702377GR114NHNSRS
Device name: Disposable Examination and Protective Nitrile Gloves Granberg®
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 4, 2025

Manufacturer & authorised representative

Manufacturer

Name: Granberg AS
SRN: NO-MF-000000207
Country: Norway
Email: post@granberg.no
Phone: +47 53775300

Variants by status

UDI-DI variants

10 UDI-DI variants

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Applied filters

basicUdiUlid01JK8ND1KQK8CSKKF16YNH7E52

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

Granberg®07023779401000
Granberg®07023771498725
Granberg®07023771498022
Granberg®07023779400805
Granberg®07023771498923
Granberg®07023771498121
Granberg®07023779400706
Granberg®07023779401109
Granberg®07023771498824
Granberg®07023779409006