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GUARDIX SG - Indonesia BPOM Medical Device Registration

GUARDIX SG is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31603325845. The device is manufactured by GENEWEL CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. PYRIDAM FARMA.

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BPOM Registered
Risk Class Kelas Resiko : D
GUARDIX SG
Analysis ID: AKL 31603325845

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

GENEWEL CO., LTD.

Country of Origin

Korea

Authorized Representative

PT. PYRIDAM FARMA

AR Address

Sinarmas MSIG Tower Lt. 12 Jl. Jenderal Sudirman Kav. 21 Kelurahan Karet

Registration Date

Aug 26, 2024

Expiry Date

Jan 30, 2028

Product Type

Surgical Equipment

Adhesion Barrier

Non Electromedic Sterile

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