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TEKNO Dilatation And Curettage Set Diagnostik - Indonesia BPOM Medical Device Registration

TEKNO Dilatation And Curettage Set Diagnostik is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11103220031. The device is manufactured by TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. TRIGELS INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : A
TEKNO Dilatation And Curettage Set Diagnostik
Analysis ID: AKL 11103220031

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

PT. TRIGELS INDONESIA

AR Address

Ruko Malaka Country Blok A No. 14, Jl. Raya Pondok Kopi RT. 009 RW. 010

Registration Date

Feb 16, 2022

Expiry Date

Jan 08, 2025

Product Type

Surgical Obstetric and Gynaecological Equipment

Obstetric-gynecologic general manual instrument.

Non Electromedic Non Sterile

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