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KAWE F.O Laryngoskop-Set Adults (REF. 03.62020.011) - Indonesia BPOM Medical Device Registration

KAWE F.O Laryngoskop-Set Adults (REF. 03.62020.011) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403812700. The device is manufactured by KAWE-KIRCHNER & WILHELM GMBH+CO., KG. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. POLARIS ALKES STARINDO.

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BPOM Registered
Risk Class Kelas Resiko : A
KAWE F.O Laryngoskop-Set Adults (REF. 03.62020.011)
Analysis ID: AKL 10403812700

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

PT. POLARIS ALKES STARINDO

AR Address

JL. Gunung Sahari Raya No. 12 G Gunung Sahari Utara, Sawah Besar

Registration Date

Sep 02, 2019

Expiry Date

Mar 25, 2024

Product Type

Therapeutic Anesthesia Equipment

Rigid laryngoscope.

Non Radiation Electromedics

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