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CELESTICA Electroencephalograph Electrode - Indonesia BPOM Medical Device Registration

CELESTICA Electroencephalograph Electrode is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21001719561. The device is manufactured by CELESTICA ELECTRONICS (S) PTE., LTD. from Singapore, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDTRONIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
CELESTICA Electroencephalograph Electrode
Analysis ID: AKL 21001719561

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Singapore

Authorized Representative

PT. MEDTRONIC INDONESIA

AR Address

Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda, Desa/Kelurahan Kebayoran Lama Utara, Kec. Kebayoran Lama

Registration Date

Nov 25, 2024

Expiry Date

Feb 20, 2029

Product Type

Diagnostic Neurology Equipment

Cutaneous electrode.

Non Radiation Electromedics

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