Singapore HSA registration DE0510534
GEUDER SZURMAN SINGLE-USE DMEK-CARTRIDGE
Singapore·CLASS B·Geuder AG·Registered April 01, 2025Device classification
- Device Class
- CLASS B
- Medical Speciality Area
- Ophthalmology
Registration information
- Registration Number
- DE0510534
- Registration Date
- April 01, 2025
- Retention Due Date
- March 31, 2026
Product description
The SZURMAN Single-Use DMEK-Cartridge is used for the therapy of corneal diseases, which only affect the corneal endothelium, as for example Fuchs endothelial dystrophy or bullous keratopathy. The SZURMAN Single-Use DMEK-Cartridge is a single-use system to implant a human donor Descemet membrane into the recipient’s eye. The transplant surgeon injects the lamella into the recipient's eye using the SZURMAN Single-Use DMEK-Cartridge. The SZURMAN Single-Use DMEK-Cartridge can be used for DMEK in children, adolescents and adults.
Product Owner
- Name
- Geuder AG
- Short Name
- Geuder AG
- Address
- Hertzstraße 4, 69126 Heidelberg, GERMANY
Registrant
- Name
- Surgipro Pte Ltd
- Address
- 23 WOODLANDS INDUSTRIAL PARK E1, ADMIRALTY INDUSTRIAL PARK, #03-05, SINGAPORE 757741
Importer
- Name
- Surgipro Pte Ltd
- Address
- 23 WOODLANDS INDUSTRIAL PARK E1, ADMIRALTY INDUSTRIAL PARK, #03-05, SINGAPORE 757741
Model information
- Model Name(s)
- SZURMAN SINGLE-USE DMEK-CARTRIDGE SZURMAN SINGLE-USE DMEK-CARTRIDGE
- Model Identifier(s)
- G-38630 G-38635
About this record
Access comprehensive regulatory information for GEUDER SZURMAN SINGLE-USE DMEK-CARTRIDGE in the Singapore medical device market through Pure Global AI's free database. This CLASS B medical device is registered under HSA registration number DE0510534 and owned by Geuder AG. The device was registered on April 01, 2025.
This page provides complete registration details including product owner information, registrant details, importer information, and regulatory compliance data from the official Singapore HSA medical device database. Pure Global AI offers free access to Singapore's complete medical device registry, helping global MedTech companies navigate HSA regulations efficiently.
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