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ULTRA V Mono PCL - Indonesia BPOM Medical Device Registration

ULTRA V Mono PCL is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603024002. The device is manufactured by SKINMEDIENCE from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. REGENESIS INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
ULTRA V Mono PCL
Analysis ID: AKL 21603024002

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

SKINMEDIENCE

Country of Origin

Korea

Authorized Representative

PT. REGENESIS INDONESIA

AR Address

Jl. Panglima Polim Raya Blok B III/107, Jakarta Selatan

Registration Date

Jul 17, 2020

Expiry Date

May 13, 2025

Product Type

Surgical Equipment

Absorbable polydioxanone surgical suture.

Non Electromedic Sterile

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