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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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SEALITE REGULAR — 2 UDI-DI variants, MDR (ACTEON MANUFACTURING)

MD Atlas
ACTEON MANUFACTURING

Data from EUDAMED, last updated May 19, 2026

SEALITE REGULAR

376024300sealiterPY

2 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: ACTEON MANUFACTURING

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Device characteristics

Implantable

Clinical investigations

Registered: No

Registered: No

Identity & classification

Basic UDI-DI: 376024300sealiterPY
Device name: SEALITE REGULAR
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 11, 2025

Manufacturer & authorised representative

Manufacturer

Name: ACTEON MANUFACTURING
SRN: FR-MF-000007556
Country: France
Email: genevieve.devilledon@acteongroup.com
Phone: +33 6 03 04 65 64

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JKT4540CRPTAJ79TRJQY60Q6

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

26626703760243000867
26626403760243000911