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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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PUD — 95 UDI-DI variants, MDR (EM EXACT, S.A.)

MD Atlas
EM EXACT, S.A.

Data from EUDAMED, last updated May 23, 2026

PUD

8445594_PUNTA_DEST_KB

95 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: EM EXACT, S.A.

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 8445594_PUNTA_DEST_KB
Device name: —
Device model: PUD
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 5, 2025

Manufacturer & authorised representative

Manufacturer

Name: EM EXACT, S.A.
SRN: ES-MF-000010830
Country: Spain
Email: j.esteba@emexact.com

Variants by status

UDI-DI variants

95 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JNGJPRBVGXVKXH7KR2BY2Q70

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

UBH0101308445594026739
656708445594001217
656608445594001194
657208445594001866
832408445594002160
601208445594001163
0844559400172908445594001729
BHS0100108445594001750
1184508445594001453
603808445594026579
602308445594001088
832108445594001835
601108445594001064
654908445594001149
603008445594001903
657608445594001323
602608445594001569
658108445594001965
603208445594001026
805708445594001538

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