AT LISA Tri 839 MP - Indonesia BPOM Medical Device Registration
AT LISA Tri 839 MP is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31202313553. The device is manufactured by CARL ZEISS MEDITEC AG. from Germany, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is ELO KARSA UTAMA.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 3
Manufacturer
CARL ZEISS MEDITEC AG.Country of Origin
Germany
Authorized Representative
ELO KARSA UTAMAAR Address
Jl. Raya Kebayoran Lama No. 34-E, Grogol Selatan, Kebayoran Lama.
Registration Date
Mar 10, 2022
Expiry Date
May 01, 2025
Product Type
Prosthetic Eye Equipment
Intraocular lens.
Non Electromedic Sterile
ZEISS OPMI Pentero 800
ZEISS RESIGHT 700
ZEISS PENTERO 800 S
ZEISS Resight
VISULAS Green Classic
VISALIS S500
VISULAS Green Comfort
ZEISS Surgical Microscope
CARL ZEISS OPMI PENTERO 800
ZEISS TIVATO 700
VISULAS Yag
CARL ZEISS MEDITEC AG
IKEGAMI Medical Grade Monitor
ORION TECHNOLOGY CO., LTD.
IKEGAMI Medical Grade Camera
IKEGAMI TSUSHINKI CO., LTD.
IKEGAMI Medical Grade Camera
IKEGAMI TSUSHINKI CO., LTD.
IKEGAMI Medical Grade Digital Video Recorder
DONGGUAN TEAC ELECTRONIC CO., LTD.
IKEGAMI Medical Grade Monitor
LG ELECTRONICS, INC.
IKEGAMI Medical Grade Monitor
IKEGAMI TSUSHINKI CO., LTD.
IKEGAMI Medical Grade Monitor
IKEGAMI TSUSHINKI CO., LTD.
ZEISS VISUCAM 224
CARL ZEISS MEDITEC AG.
ZEISS TRENION 3D HD
CARL ZEISS MEDITEC AG

