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ANKIYA Single Use Oxygen Prefilled Humidifier - Indonesia BPOM Medical Device Registration

ANKIYA Single Use Oxygen Prefilled Humidifier is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403420219. The device is manufactured by ANKIYA BIO TEC CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is INDOWELL MEDTECH INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
ANKIYA Single Use Oxygen Prefilled Humidifier
Analysis ID: AKL 20403420219

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

INDOWELL MEDTECH INDONESIA

AR Address

Ruko Apartemen City Home, Jalan Raya Boulevard Blok M56, Rt.006/Rw.019, Desa/Kelurahan Kelapa Gading Timur, Kec. Kelapa Gading, Kota Adm. Jakarta Utara, Provinsi DKI Jakarta, Kode Pos: 14240

Registration Date

Mar 14, 2024

Expiry Date

Jan 01, 2029

Product Type

Therapeutic Anesthesia Equipment

Respiratory gas humidifier.

Non Electromedic Sterile

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