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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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Dallop NM, Dallop NM ULTRALIGHT — 4 UDI-DI variants, MDR

MD Atlas
TRICOMED S.A.

Data from EUDAMED, last updated May 30, 2026

Dallop NM, Dallop NM ULTRALIGHT

59061465FFKXXXXXF

4 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Manufacturer: TRICOMED S.A.

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Device characteristics

Implantable

Legacy certificates

Certificate number: 1434-MDR-008/2024
Type: refdata.certificate-mdr-type.technical-documentation
Notified body: POLSKIE CENTRUM BADAN I CERTYFIKACJI S.A. (1434)
Validity: Sep 5, 2024 → Jul 11, 2029

Identity & classification

Basic UDI-DI: 59061465FFKXXXXXF
Device name: Dallop NM, Dallop NM ULTRALIGHT
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Version date: Jul 30, 2024

Manufacturer & authorised representative

Manufacturer

Name: TRICOMED S.A.
SRN: PL-MF-000002483
Country: Poland
Email: sekretariat@tricomed.com
Phone: +48 42 689 65 20

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01J41431G2S9TM7H3VATFDYG71

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

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