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BUMI Uterine Manipulator - Indonesia BPOM Medical Device Registration

BUMI Uterine Manipulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21103320627. The device is manufactured by SEJONG MEDICAL CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SOMETECH NEW Zealand.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
BUMI Uterine Manipulator
Analysis ID: AKL 21103320627

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

SOMETECH NEW Zealand

AR Address

AKR Tower Lantai 11 Unit 11G dan 11C, Jalan Panjang Nomor 5 ,RT 011 RW 010, Kec. Kebon Jeruk, Kel. Kebon Jeruk, Jakarta Barat, 11530

Registration Date

Oct 27, 2023

Expiry Date

Jun 16, 2028

Product Type

Surgical Obstetric and Gynaecological Equipment

Obstetric-gynecologic specialized manual instrument.

Non Electromedic Sterile

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