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ENDOLASER 422 - Indonesia BPOM Medical Device Registration

ENDOLASER 422 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603113532. The device is manufactured by ENRAF NONIUS B.V. from Netherlands, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MURTI INDAH SENTOSA.

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
ENDOLASER 422
Analysis ID: AKL 21603113532

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

ENRAF NONIUS B.V.

Country of Origin

Netherlands

Authorized Representative

PT. MURTI INDAH SENTOSA

AR Address

WISMA MURTI JL. SULTAN ISKANDAR MUDA KAV. 29 ARTERI PONDOK INDAH

Registration Date

Jun 13, 2019

Expiry Date

Nov 28, 2023

Product Type

Surgical Equipment

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

Non Radiation Electromedics

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