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JUVELOOK - Indonesia BPOM Medical Device Registration

JUVELOOK is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602420097. The device is manufactured by SPIRIT CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is SMELL MEDICAL INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : D
JUVELOOK
Analysis ID: AKL 31602420097

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

SPIRIT CO., LTD

Country of Origin

Korea

Authorized Representative

SMELL MEDICAL INDONESIA

AR Address

Gedung Tifa Arum Realty Lt.8, Suite 801 Jl. Kuningan Barat 1 No. 26, Kelurahan Kuningan Barat, Kecamatan Mampang Prapatan. Jakarta Selatan, DKI Jakarta

Registration Date

Jul 29, 2024

Expiry Date

Apr 19, 2029

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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