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EAGLECARE Surgical Light - Indonesia BPOM Medical Device Registration

EAGLECARE Surgical Light is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603911652. The device is manufactured by NANJING DINRI MEDICAL CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INAHO JAYA LESTARI.

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
EAGLECARE Surgical Light
Analysis ID: AKL 21603911652

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. INAHO JAYA LESTARI

AR Address

Jl. Tentara Pelajar No. 42 - 42A

Registration Date

Mar 31, 2022

Expiry Date

Mar 30, 2025

Product Type

Surgical Equipment

Surgical lamp.

Non Radiation Electromedics

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