KARMI Blood Bag - Indonesia BPOM Medical Device Registration
KARMI Blood Bag is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209814387. The device is manufactured by KAWASUMI LABORATORIES (THAILAND) CO., LTD. from Thailand, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FRISMED HOSLAB INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
KAWASUMI LABORATORIES (THAILAND) CO., LTD.Country of Origin
Thailand
Authorized Representative
PT. FRISMED HOSLAB INDONESIAAR Address
Ruko Bidex Blok G No. 30-31 Jl. Pahlawan Seribu BSD City, 15321
Registration Date
Jun 27, 2023
Expiry Date
Oct 01, 2026
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Empty container for the collection and processing of blood and blood components.
Non Electromedic Sterile
KARMI Blood Bag
KAWASUMI LABORATORIES (THAILAND) CO., LTD.
KARMI Blood Bag
KAWASUMI LABORATORIES (THAILAND) CO., LTD.
KARMI Blood Bag
KAWASUMI LABORATORIES (THAILAND) CO., LTD.
KARMI Blood Bag
KAWASUMI LABORATORIES (THAILAND) CO., LTD.
KARMI Blood Bag
KAWASUMI LABORATORIES (THAILAND) CO., LTD.
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