241118

Cataract Extraction Phacoemulsification/Vitrectomy Systems

白内障摘除超声乳化术/玻璃体切除术系统
Johnson & Johnson Surgical Vision, Inc.·III·Hong Kong MDACS·Registered October 16, 2024
Device overview
Risk class
III
Product code
27995
State
current
Status
N/A
Product code detail
27995 Cataract Extraction Phacoemulsification/Vitrectomy Systems
Manufacturer (製造商)
Name
Johnson & Johnson Surgical Vision, Inc.
Johnson & Johnson Medtech
Country
United States
美国
Address
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)
Phone
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)
About this record

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