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SP DYNAMIS - Indonesia BPOM Medical Device Registration

SP DYNAMIS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603911936. The device is manufactured by PHOTONA D.O.O. from Slovenia, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ADMIRAL BLESENSA IMMORTAL.

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 : C
SP DYNAMIS
Analysis ID: AKL 21603911936

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

PHOTONA D.O.O.

Country of Origin

Slovenia

Authorized Representative

PT. ADMIRAL BLESENSA IMMORTAL

AR Address

Ruko Graha Handaya unit H Jl. Raya Pejuangan Kav. 12A, Kebon Jeruk, Kota Jakarta Barat, Kode Pos 11530

Registration Date

Sep 12, 2023

Expiry Date

Jul 27, 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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