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PORTEX Epidural Minipack System 1 - Indonesia BPOM Medical Device Registration

PORTEX Epidural Minipack System 1 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403514662. The device is manufactured by SMITHS MEDICAL CZECH REPUBLIC A.S. from Czech Republic, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. IDS MEDICAL SYSTEMS INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
PORTEX Epidural Minipack System 1
Analysis ID: AKL 20403514662

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Czech Republic

Authorized Representative

PT. IDS MEDICAL SYSTEMS INDONESIA

AR Address

Gedung Wisma 76, Lantai 17 & 22, Jl. LetJend. S. Parman Kav.76, Kelurahan Slipi, Kecamatan Palmerah, 11410

Registration Date

Jun 04, 2020

Expiry Date

Mar 16, 2025

Product Type

Therapeutic Anesthesia Equipment

Anesthesia conduction kit.

Non Electromedic Sterile

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