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MORTON Silicone Reusable Manual Artificial Resuscitation Bag - Indonesia BPOM Medical Device Registration

MORTON Silicone Reusable Manual Artificial Resuscitation Bag is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403510775. The device is manufactured by MORTON MEDICAL LTD. from Turkey, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ALKESTRON SELF-SOURCE.

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BPOM Registered
Risk Class Kelas Resiko : B
MORTON Silicone Reusable Manual Artificial Resuscitation Bag
Analysis ID: AKL 20403510775

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Turkey

Authorized Representative

PT. ALKESTRON SELF-SOURCE

AR Address

Komp Ruko Griya Inti Sentosa Jln. Griya Agung Blok O No. 95-96

Registration Date

Jul 17, 2019

Expiry Date

Mar 05, 2024

Product Type

Therapeutic Anesthesia Equipment

Manual emergency ventilator.

Non Electromedic Non Sterile

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