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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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Biopsy Punch — 7 UDI-DI variants, MDR

MD Atlas
GlaxoSmithKline Trading Services Limited

Data from EUDAMED, last updated May 24, 2026

Biopsy Punch

5054363591190830BZ

7 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: GlaxoSmithKline Trading Services Limited

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5054363591190830BZ
Device name: Biopsy Punch
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: GlaxoSmithKline Trading Services Limited
SRN: IE-MF-000008351
Country: Ireland
Email: PSC.MDT-Approvals@gsk.com
Phone: 353-14955000

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01KRX8XNZDC0T0B9FJ25T090FN

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

8975585054363000383
8975485054363000376
8975385054363000307
8975685054363000369
8975785054363000352
8975885054363000345
8975985054363000338