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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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Scleral knife / Lance sclerali — 5 UDI-DI variants, MDR (AKTIVE SRL)

MD Atlas
AKTIVE SRL

Data from EUDAMED, last updated May 30, 2026

Scleral knife / Lance sclerali

8052276FT0002ID5CP

5 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: AKTIVE SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8052276FT0002ID5CP
Device name: Scleral knife / Lance sclerali
Device model: Scleral knife / Lance sclerali
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Dec 12, 2022

Manufacturer & authorised representative

Manufacturer

Name: AKTIVE SRL
SRN: IT-MF-000007813
Country: Italy
Email: quality@aktive-corp.com
Phone: 06.88640509

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01GM2XV5SA4BGJAQNFSK84YK02

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

Scleral blade 19G08052276019530
Scleral blade 20G08052276019554
Scleral blade 23G08052276019578
Scleral blade 25G08052276019592
Scleral blade 27G08052276019516