PHYSIOMER HYPERTONIC - Indonesia BPOM Medical Device Registration

PHYSIOMER HYPERTONIC is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20704022525. The device is manufactured by LABORATORY OF THE SEA from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ISCO LOGISTICS INDONESIA.

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BPOM Registered

Risk Class Kelas Resiko : B

PHYSIOMER HYPERTONIC

Analysis ID: AKL 20704022525

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

LABORATORY OF THE SEA

Country of Origin

France

Authorized Representative

PT. ISCO LOGISTICS INDONESIA

AR Address

JL. H.R. MOCH. MANGUNDIPROJO NO. 1A

Registration Date

Nov 29, 2024

Expiry Date

May 21, 2029

Product Type

Therapeutic Ear, Nose and Throat Equipment

Nasal irrigation solution

Non Electromedic Sterile

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Other Products from LABORATORY OF THE SEA

Products from the same manufacturer (10 products)

FARLING INDUSTRIAL CO., LTD.

Kelas Resiko : A

PHYSIOMER HYPERTONIC - Indonesia BPOM Medical Device Registration

Risk Classification

Product Class

Manufacturer

Country of Origin

Authorized Representative

AR Address

Registration Date

Expiry Date

Product Type

DJ Fang

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