FOREMOUNT – Nasal Airway - Indonesia BPOM Medical Device Registration

FOREMOUNT – Nasal Airway is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403420639. The device is manufactured by FOREMOUNT ENTERPRISE CO., LTD from Taiwan (China), and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. LABORA MANDIRI INDO PRATAMA.

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BPOM Registered

Risk Class Kelas Resiko : A

FOREMOUNT – Nasal Airway

Analysis ID: AKL 10403420639

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

FOREMOUNT ENTERPRISE CO., LTD

Country of Origin

Taiwan (China)

Authorized Representative

PT. LABORA MANDIRI INDO PRATAMA

AR Address

Jl. C. Simanjuntak No. 47, RT.014, RW.003, Desa/Kelurahan Terban, Kecamanan Gondokusuman, Kota Yogyakarta, Provinsi Daerah Istimewa Yogyakarta, Kode Pos : 55223

Registration Date

Sep 27, 2024

Expiry Date

Apr 06, 2027

Product Type

Therapeutic Anesthesia Equipment

Nasopharyngeal airway

Non Electromedic Non Sterile

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Products from the same manufacturer (10 products)

FOREMOUNT – Nasal Airway - Indonesia BPOM Medical Device Registration

Risk Classification

Product Class

Manufacturer

Country of Origin

Authorized Representative

AR Address

Registration Date

Expiry Date

Product Type

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