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COVALON CoIActive Plus - Indonesia BPOM Medical Device Registration

COVALON CoIActive Plus is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31603022244. The device is manufactured by BARIL CORPORATION from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is SEKARGUNA MEDIKA.

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BPOM Registered
Risk Class Kelas Resiko : D
COVALON CoIActive Plus
Analysis ID: AKL 31603022244

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

BARIL CORPORATION

Country of Origin

United States

Authorized Representative

SEKARGUNA MEDIKA

AR Address

jl.Ciputat Raya no 14 B.Pondok Pinang

Registration Date

Apr 22, 2020

Expiry Date

Jul 10, 2024

Product Type

Surgical Equipment

Absorbable hemostatic agent and dressing.

Non Electromedic Sterile

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