LANLING OTOSCOPE - Indonesia BPOM Medical Device Registration
LANLING OTOSCOPE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10703914548. The device is manufactured by SUZHOU KANGJIE MEDICAL INC. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ARITEK KARYA MANDIRI.
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 : 1
Manufacturer
SUZHOU KANGJIE MEDICAL INC.Country of Origin
China
Authorized Representative
PT. ARITEK KARYA MANDIRIAR Address
Green Lake City Rukan Crown Blok. A No. 19 Kelurahan Petir, Kecamatan Cipondoh Tangerang, Banten
Registration Date
Nov 02, 2023
Expiry Date
Dec 13, 2025
Product Type
Ear, Nose and Throat Surgical Equipment
Otoscope.
Non Radiation Electromedics
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