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Dr. OPPEL Electrosurgical unit - Indonesia BPOM Medical Device Registration

Dr. OPPEL Electrosurgical unit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603022547. The device is manufactured by SOMETECH INC. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SOMETECH NEW Zealand.

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BPOM Registered
Risk Class Kelas Resiko : C
Dr. OPPEL Electrosurgical unit
Analysis ID: AKL 21603022547

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

SOMETECH INC.

Country of Origin

Korea

Authorized Representative

PT. 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

Jan 17, 2025

Expiry Date

Dec 12, 2029

Product Type

Surgical Equipment

Electrosurgical cutting and coagulation device and accessories.

Non Radiation Electromedics

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