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PENTAX MEDICAL LARYNGEAL STROBE - Indonesia BPOM Medical Device Registration

PENTAX MEDICAL LARYNGEAL STROBE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20703021857. The device is manufactured by PENTAX OF AMERICA, INC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PRO-HEALTH INTERNATIONAL.

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BPOM Registered
Risk Class Kelas Resiko : B
PENTAX MEDICAL LARYNGEAL STROBE
Analysis ID: AKL 20703021857

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. PRO-HEALTH INTERNATIONAL

AR Address

Komplek Perkantoran Duta Merlin Blok C 35-36, Jl. Gajah Mada 3-5 RT 002 RW 005, Prov. DKI Jakarta, Kota Jakarta Pusat, Kec. Gambir, Kel. Petojo Utara

Registration Date

Sep 03, 2024

Expiry Date

Jul 23, 2027

Product Type

Ear, Nose and Throat Surgical Equipment

Laryngostroboscope.

Non Radiation Electromedics

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