LAMEDITECH HandyRay Laser Lancing Device - Indonesia BPOM Medical Device Registration
LAMEDITECH HandyRay Laser Lancing Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603323877. The device is manufactured by LAMEDITECH CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MULTISERA INDOSA.
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 : 2
Manufacturer
LAMEDITECH CO., LTD.Country of Origin
Korea
Authorized Representative
PT. MULTISERA INDOSAAR Address
JL. JEND. SUDIRMAN NO. 689 RT/RW : 21/07
Registration Date
Apr 28, 2023
Expiry Date
Dec 01, 2025
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
Non Electromedic Sterile
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