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GE SEER 1000 Multi Channel Digital Holter Recorder - Indonesia BPOM Medical Device Registration

GE SEER 1000 Multi Channel Digital Holter Recorder is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502411461. The device is manufactured by GETEMED MEDIZIN UND INFORMATIONSTECHNIK AG. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GE OPERATIONS INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
GE SEER 1000 Multi Channel Digital Holter Recorder
Analysis ID: AKL 20502411461

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. GE OPERATIONS INDONESIA

AR Address

South Quarter Tower B, Lantai 18-19, JL. R.A. Kartini Kav. 8, Kelurahan Cilandak Barat, Kecamatan Cilandak, Kota Adm. Jakarta Selatan, Provinsi DKI Jakarta, 12430

Registration Date

Feb 13, 2024

Expiry Date

Dec 11, 2028

Product Type

Monitoring Cardiology Equipment

Medical magnetic tape recorder.

Non Radiation Electromedics

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