241118
III
current
Cataract Extraction Phacoemulsification/Vitrectomy Systems白内障摘除超声乳化术/玻璃体切除术系统
This profile provides complete Hong Kong MDACS registration information for Cataract Extraction Phacoemulsification/Vitrectomy Systems. Review device classification, authorised representative (AR) details, manufacturer contacts, product codes, and regulatory milestones. Pure Global AI delivers bilingual transparency for medical device registrations across Asia.
Product Info: Cataract Extraction Phacoemulsification/Vitrectomy Systems
產品資訊： 白内障摘除超声乳化术/玻璃体切除术系统
Device Overview
Hong Kong MDACS registration summary and classification details.
Risk Class
III
Product Code
27995
Product Code Detail
27995 Cataract Extraction Phacoemulsification/Vitrectomy Systems
State
current
Status
N/A
Manufacturer (製造商)
Johnson & Johnson Surgical Vision, Inc.
Johnson & Johnson Medtech
United States
美国
31 Technology Drive, Suite 200, Irvine, CA 92618, United States of America
31 Technology Drive, Suite 200, Irvine, CA 92618, 美国
Authorised Representative (AR)
24803330
Regulatory Timeline
Registration Date
October 16, 2024
Expiry Date
October 15, 2029
Product Models
VERITAS Vision System Console (VRT680300), VERITAS Remote Control (VRT680135), VERITAS Foot Pedal (VRT680700), VERITAS Swivel Phaco handpiece (VRT691027), VERITAS Advanced Infusion Pack (GFI) (VRT-AI), VERITAS Advanced Fluidics Pack (NonGFI) (VRT-AF), LAMINAR Flow Phaco Tip and Irrigation Sleeve (OPOR1519L, OPOR3019L, OPOR4519L)
VERITAS 视觉系统控制台 (VRT680300)、VERITAS 遥控器 (VRT680135)、VERITAS 脚踏板 (VRT680700)、VERITAS 旋转式超声乳清手机 (VRT691027)、VERITAS 高级输液套装 (GFI) (VRT-AI)、VERITAS 高级液流套装 (NonGFI) (VRT-AF)、层流超声诊断尖端和冲洗套管 (OPOR1519L、OPOR3019L、OPOR4519L)