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Flexilux II Laparoscope - Indonesia BPOM Medical Device Registration

Flexilux II Laparoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21106913546. The device is manufactured by SCHOLLY FIBEROPTIC, GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDTRONIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
Flexilux II Laparoscope
Analysis ID: AKL 21106913546

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. MEDTRONIC INDONESIA

AR Address

Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda

Registration Date

May 31, 2019

Expiry Date

Apr 11, 2024

Product Type

Diagnostic Obstetric and Gynaecological Equipment

Gynecologic laparoscope and accessories.

Non Electromedic Non Sterile

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