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CERKAMED Alustat Foam - Indonesia BPOM Medical Device Registration

CERKAMED Alustat Foam is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31603422137. The device is manufactured by PPH CERKAMED WOJCIECH PAWLOWSKI from Poland, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is THOMASONG NIRMALA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : D
CERKAMED Alustat Foam
Analysis ID: AKL 31603422137

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Poland

Authorized Representative

THOMASONG NIRMALA

AR Address

Jl. AM. Sangaji No. 20A

Registration Date

Sep 13, 2024

Expiry Date

Oct 13, 2027

Product Type

Surgical Equipment

Absorbable hemostatic agent and dressing.

Non Electromedic Non Sterile

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