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ULTRA V EZ CANNULA (PCL 360° COG) LC-SM - Indonesia BPOM Medical Device Registration

ULTRA V EZ CANNULA (PCL 360° COG) LC-SM is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603125264. 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 EZ CANNULA (PCL 360° COG) LC-SM
Analysis ID: AKL 21603125264

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

SKINMEDIENCE

Country of Origin

Korea

Authorized Representative

PT. REGENESIS INDONESIA

AR Address

Jl. Sultan Iskandar Muda No. 7A & B

Registration Date

Aug 29, 2021

Expiry Date

Dec 02, 2025

Product Type

Surgical Equipment

Absorbable polydioxanone surgical suture.

Non Electromedic Sterile

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