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LAVIEEN - Indonesia BPOM Medical Device Registration

LAVIEEN is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603325164. The device is manufactured by WON TECH CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is SOMETECH NEW Zealand.

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
LAVIEEN
Analysis ID: AKL 21603325164

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

WON TECH CO., LTD.

Country of Origin

Korea

Authorized Representative

SOMETECH NEW Zealand

AR Address

AKR Tower Lantai 11 Unit 11G dan 11C, Jalan Panjang Nomor 5 ,RT 011 RW 010, Kec. Kebon Jeruk, Kel. Kebon Jeruk, Jakarta Barat, 11530

Registration Date

Oct 04, 2023

Expiry Date

Aug 16, 2028

Product Type

Surgical Equipment

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

Non Radiation Electromedics

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