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GEA Neonate Bilirubin Phototherapy Equipment - Indonesia BPOM Medical Device Registration

GEA Neonate Bilirubin Phototherapy Equipment is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902420621. The device is manufactured by NINGBO DAVID MEDICAL DEVICE CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEGA PRATAMA MEDICALINDO.

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BPOM Registered
Risk Class Kelas Resiko : B
GEA Neonate Bilirubin Phototherapy Equipment
Analysis ID: AKL 20902420621

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. MEGA PRATAMA MEDICALINDO

AR Address

Jl. Pluit Raya 133 Blok A.3

Registration Date

Jun 21, 2024

Expiry Date

Jun 02, 2026

Product Type

Therapeutic General and Individual Hospital Equipment

Neonatal phototherapy unit.

Non Radiation Electromedics

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DJ Fang

DJ Fang

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