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FIEGERT-ENDOTECH Urethrotomy Instrument Set - Indonesia BPOM Medical Device Registration

FIEGERT-ENDOTECH Urethrotomy Instrument Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10801311979. The device is manufactured by FIEGERT ENDOTECH MEDIZINTECHNIK GMBH. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. PRIMARY WORKS.

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BPOM Registered
Risk Class Kelas Resiko : A
FIEGERT-ENDOTECH Urethrotomy Instrument Set
Analysis ID: AKL 10801311979

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

PT. PRIMARY WORKS

AR Address

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

Registration Date

Oct 17, 2021

Expiry Date

Nov 27, 2025

Product Type

Gastroenterology-Surgical Urology Equipment

Manual gastroenterology-urology surgical instrument and accessories.

Non Electromedic Non Sterile

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