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KARL KAPS AS Colposcope - Indonesia BPOM Medical Device Registration

KARL KAPS AS Colposcope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21106610649. The device is manufactured by KARL KAPS GMBH & CO., KG. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is BETA MEDICAL.

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Risk Class Kelas Resiko : B
KARL KAPS AS Colposcope

KARL KAPS SOM Colposcope

Analysis ID: AKL 21106610649

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

BETA MEDICAL

AR Address

Jl. Pangeran Antasari No. 212

Registration Date

Jan 24, 2022

Expiry Date

Sep 06, 2026

Product Type

Diagnostic Obstetric and Gynaecological Equipment

Colposcope.

Non Radiation Electromedics

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