350-252Ophthalmic Cryosurgery System
Argentina Medical Device Registration · KEELER · CENTRO OPTICO CASIN S.A. · Registered October 09, 2023
Revalidation of Registration I-II-III-IV- Registration Type
- Revalidation of Registration I-II-III-IV
- Reválida de Registro I-II-III-IV
- Product Code
- 350-252
- Brand Name
- KEELER
- Product Name
- Ophthalmic Cryosurgery System
- Sistema para Criocirugía Oftálmica
- Registration Date
- October 09, 2023
- Database ID
- cmhazbf7z0dobekwi8322eria
2509-P-1010 Cryomatic System for Surgery Probes: 2508-P-7022 Disposable retinal probe, standard, 2.5mm, for cryosurgery, box of 10 2509-P-8020 Standard Retinal Probe, 2.5mm, for Cryomatic MKII System 2509-P-8021 Elongated retinal probe, 2.5mm, for Cryomatic MKII system 2509-P-8022 Sonsa retinal medium range, 2.5mm, for Cryomatic MKII system 2509-P-8023 Intravitreal retinal probe for Cryomatic MKII system 2509-P-8024 Curved cataract probe, 1.5mm, for Cryomatic MKII system 2509-P-8025 Glaucoma probe, 3mm, for Cryomatic MKII system 2509-P-8026 Collins Trichiasis Probe, 4 x 10 mm, for Cryomatic MKII System 2509-P-8030 Classic retinal probe
2509-P-1010 Sistema Cryomatic para cirugía Sondas: 2508-P-7022 Sonda retinal descartable, estándar, 2.5mm, para criocirugía, caja de 10 2509-P-8020 Sonda retinal estándar, 2.5mm, para sistema Cryomatic MKII 2509-P-8021 Sonda retinal alargada, 2.5mm, para sistema Cryomatic MKII 2509-P-8022 Sonsa retinal de medio alcance, 2.5mm, para sistema Cryomatic MKII 2509-P-8023 Sonda retinal intravitreal para sistema Cryomatic MKII 2509-P-8024 Sonda curvada para cataratas, 1.5mm, para sistema Cryomatic MKII 2509-P-8025 Sonda para glaucoma, 3mm, para sistema Cryomatic MKII 2509-P-8026 Sonda Collins para triquiasis, 4 x 10 mm, para sistema Cryomatic MKII 2509-P-8030 Sonda retinal clásica (classic)
Access comprehensive regulatory information for Ophthalmic Cryosurgery System in the Argentina medical device market through Pure Global AI's free database. This Revalidation of Registration I-II-III-IV medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on October 09, 2023.
This page provides complete registration details including product code (350-252), brand name (KEELER), authorized representative information, registration type, and regulatory compliance data from the official Argentina ANMAT medical device database. Pure Global AI offers free access to Argentina's medical device registry, helping global MedTech companies navigate Argentina regulations efficiently.