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UROLASE SP+ Laser Surgical Device - Indonesia BPOM Medical Device Registration

UROLASE SP+ Laser Surgical Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603325680. The device is manufactured by IRE-POLUS LTD. from Russia, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRITRA PRIMA INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
UROLASE SP+ Laser Surgical Device
Analysis ID: AKL 21603325680

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

IRE-POLUS LTD.

Country of Origin

Russia

Authorized Representative

PT. TRITRA PRIMA INDONESIA

AR Address

Central Park Cikarang Blok A1 No. 02

Registration Date

Dec 05, 2023

Expiry Date

Sep 25, 2028

Product Type

Surgical Equipment

Laser surgical instrument for use in general and plastic surgery and in dermatology.

Non Radiation Electromedics

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