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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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Ophthalmic Microsurgical Knife, non… — 1 UDI-DI variant, MDR

MD Atlas
SURGICON AG

Data from EUDAMED, last updated May 31, 2026

Ophthalmic Microsurgical Knife, non sterile, bulk

764998830894711SNGJ

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: SURGICON AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 764998830894711SNGJ
Device name: Ophthalmic Microsurgical Knife, non sterile, bulk
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: SURGICON AG
SRN: CH-MF-000020566
Country: Switzerland
Email: info@surgicon.ch

Authorised representative

Name: Advena Limited
SRN: MT-AR-000000234
Country: Malta

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KSP9FM5FCFZJC9R9REXNX11V

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

SURGICUT Straight Knife 15°07640232561219