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LKTECH HIFU ULTRAFOCUS - Indonesia BPOM Medical Device Registration

LKTECH HIFU ULTRAFOCUS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603422528. The device is manufactured by GUANGZHOU SUNWIN TECHNOLOGY CO. LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. JAMBERDETAK DERMA TECH.

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BPOM Registered
Risk Class Kelas Resiko : B
LKTECH HIFU ULTRAFOCUS
Analysis ID: AKL 21603422528

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. JAMBERDETAK DERMA TECH

AR Address

Komplek Pakuan, Villa Intan Pakuan II Nomor 2

Registration Date

Oct 28, 2024

Expiry Date

Oct 27, 2027

Product Type

Surgical Equipment

Focused ultrasound stimulator system for aesthetic use

Non Radiation Electromedics

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