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SUNMED Conventional Laryngoscope Set - Indonesia BPOM Medical Device Registration

SUNMED Conventional Laryngoscope Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403815383. The device is manufactured by SUNMED LLC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ANDRA PRIMA JAYA.

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BPOM Registered
Risk Class Kelas Resiko : A
SUNMED Conventional Laryngoscope Set
Analysis ID: AKL 10403815383

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

SUNMED LLC.

Country of Origin

United States

Authorized Representative

PT. ANDRA PRIMA JAYA

AR Address

JL. TANAH ABANG III NO. 19E KEL. PETOJO SELATAN KEC. GAMBIR

Registration Date

Dec 13, 2023

Expiry Date

Jun 30, 2027

Product Type

Therapeutic Anesthesia Equipment

Rigid laryngoscope.

Non Electromedic Sterile

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