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SINUSORB PGA Suture - Indonesia BPOM Medical Device Registration

SINUSORB PGA Suture is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603222171. The device is manufactured by PETERS SURGICAL from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is GLOBAL DISPOMEDIKA.

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BPOM Registered
Risk Class Kelas Resiko : C
SINUSORB PGA Suture
Analysis ID: AKL 21603222171

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

PETERS SURGICAL

Country of Origin

France

Authorized Representative

GLOBAL DISPOMEDIKA

AR Address

Jl. Penjernihan 1 No. 38 Lt. 2

Registration Date

Aug 31, 2024

Expiry Date

Dec 31, 2028

Product Type

Surgical Equipment

Absorbable poly(glycolide/ l -lactide) surgical suture.

Non Electromedic Sterile

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