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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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Procedure Pack for Corneal Surgery 8.5… — 32 UDI-DI variants, MDR

MD Atlas
SIE AG, Surgical Instrument Engineering

Data from EUDAMED, last updated May 23, 2026

Procedure Pack for Corneal Surgery 8.5 mm

764016775PPACKSKP

32 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: SIE AG, Surgical Instrument Engineering

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 764016775PPACKSKP
Device name: Procedure Pack for Corneal Surgery 8.5 mm
Device model: Procedure Pack for Corneal Surgery 8.5 mm
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 11, 2026

Manufacturer & authorised representative

Manufacturer

Name: SIE AG, Surgical Instrument Engineering
SRN: CH-MF-000025018
Country: Switzerland
Email: quality.ziemergroup@ziemergroup.com
Phone: +41323327050

Authorised representative

Name: Ziemer Ophthalmology (DE) GmbH
SRN: DE-AR-000005638
Country: Germany
Phone: +49 7666 90280-0

Variants by status

UDI-DI variants

32 UDI-DI variants

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basicUdiUlid01KKE159REC7KKPG5K7C3YHWFT

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

No registered UDI-DI variants for this device family.