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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

601908445594001514
834308445594001996
655708445594001552
864708445594026616
UBH0101108445594026715
655008445594001255
657008445594001682
657308445594001071
603408445594026531
UBH0100108445594001118
1184408445594001293
603508445594026548
657908445594001101
656808445594001361
1184308445594001279
655408445594001798
657808445594001613
832308445594001378
658708445594001385
865108445594026524
658308445594001422
678408445594001354
658408445594001507
864608445594026500
657708445594001491

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