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PRIMELASE - Indonesia BPOM Medical Device Registration

PRIMELASE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603917748. The device is manufactured by HIGH TECHNOLOGY PRODUCTS, S. L. U. from Spain, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ISCO LOGISTICS INDONESIA.

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.

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BPOM Registered
Risk Class Kelas Resiko : C
PRIMELASE
Analysis ID: AKL 21603917748

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Spain

Authorized Representative

PT. ISCO LOGISTICS INDONESIA

AR Address

JL. H.R. MOCH. MANGUNDIPROJO NO. 1A

Registration Date

Nov 29, 2019

Expiry Date

May 20, 2024

Product Type

Surgical Equipment

Laser surgical instrument for use in general and plastic surgery and in dermatology.

Non Radiation Electromedics

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