KEEWELL – Forced-Air Patient Warming Unit - Indonesia BPOM Medical Device Registration
KEEWELL – Forced-Air Patient Warming Unit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20505320264. The device is manufactured by KEEWELL MEDICAL TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is LABORA MANDIRI INDO PRATAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
KEEWELL MEDICAL TECHNOLOGY CO., LTDCountry of Origin
China
Authorized Representative
LABORA MANDIRI INDO PRATAMAAR Address
Jl. C. Simanjuntak No. 47
Registration Date
Aug 28, 2023
Expiry Date
Feb 09, 2026
Product Type
Therapeutic Cardiology Equipment
Thermal regulating system.
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