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HP Vitaran - Indonesia BPOM Medical Device Registration

HP Vitaran is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602420042. The device is manufactured by BR PHARM 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
HP Vitaran
Analysis ID: AKL 31602420042

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

BR PHARM 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

May 06, 2024

Expiry Date

Oct 30, 2028

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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