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Suprasorb H - Indonesia BPOM Medical Device Registration

Suprasorb H is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603120611. The device is manufactured by URGO LABORATORIES from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. NUSA ASIA MEDIKA.

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BPOM Registered
Risk Class Kelas Resiko : B
Suprasorb H
Analysis ID: AKL 21603120611

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

URGO LABORATORIES

Country of Origin

France

Authorized Representative

PT. NUSA ASIA MEDIKA

AR Address

Rukan CBD, Green Lake City F No. 15 Ketapang. Cipondoh

Registration Date

Feb 01, 2021

Expiry Date

Mar 01, 2025

Product Type

Surgical Equipment

Hydrophilic wound dressing

Non Electromedic Sterile

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