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FIEGERT-ENDOTECH Hand Instrument Laparoscopy Set - Indonesia BPOM Medical Device Registration

FIEGERT-ENDOTECH Hand Instrument Laparoscopy Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801810363. The device is manufactured by FIEGERT ENDOTECH MEDIZINTECHNIK GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PRIMARY WORKS.

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BPOM Registered
Risk Class Kelas Resiko : B
FIEGERT-ENDOTECH Hand Instrument Laparoscopy Set
Analysis ID: AKL 20801810363

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PRIMARY WORKS

AR Address

Daan Mogot Arcadia Blok F.1/8A-8B Jl. Daan Mogot Km 21, Kelurahan Batu Ceper

Registration Date

Sep 10, 2021

Expiry Date

Dec 31, 2025

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories.

Non Electromedic Non Sterile

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