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FORSCH MEDICAL Endotracheal Tube - Indonesia BPOM Medical Device Registration

FORSCH MEDICAL Endotracheal Tube is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403818049. The device is manufactured by HANGZHOU TAPPA MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DWIASRI GRAHA.

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BPOM Registered
Risk Class Kelas Resiko : B
FORSCH MEDICAL Endotracheal Tube
Analysis ID: AKL 20403818049

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. DWIASRI GRAHA

AR Address

Jalan Utan Kayu Raya No.19A Jakarta Timur

Registration Date

Oct 20, 2021

Expiry Date

Oct 21, 2024

Product Type

Therapeutic Anesthesia Equipment

Tracheal tube.

Non Electromedic Sterile

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