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AMBU SPUR II Resuscitator - Indonesia BPOM Medical Device Registration

AMBU SPUR II Resuscitator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403420168. The device is manufactured by AMBU., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. AMI MEDIKA INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
AMBU SPUR II Resuscitator
Analysis ID: AKL 20403420168

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

AMBU., LTD.

Country of Origin

China

Authorized Representative

PT. AMI MEDIKA INDONESIA

AR Address

The Savoy B1-30, Jakarta Garden City Boulevard

Registration Date

Mar 06, 2024

Expiry Date

Aug 31, 2028

Product Type

Therapeutic Anesthesia Equipment

Manual emergency ventilator.

Non Electromedic Non Sterile

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