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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

BHS0100508445594001934
602208445594001958
UBH0100208445594001286
833108445594001224
832008445594001811
865008445594026630
603108445594001927
864508445594026494
831808445594001637
603708445594026562
657508445594001248
655608445594001972
864808445594026623
602108445594001873
UBH0101208445594026722
655308445594001675
601808445594001699
658008445594001125
658608445594002122
655808445594001736
UBH0100308445594001460
678508445594001392
601408445594001231
832208445594001200
658208445594001040

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