KEEWELL Blood & Infusion Warmer - Indonesia BPOM Medical Device Registration
KEEWELL Blood & Infusion Warmer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209812117. 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 PT. LABORA MANDIRI INDO PRATAMA.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
KEEWELL MEDICAL TECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
PT. LABORA MANDIRI INDO PRATAMAAR Address
Jl. C. Simanjuntak No. 47
Registration Date
May 11, 2023
Expiry Date
Feb 09, 2026
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Blood and plasma warming device.
Non Radiation Electromedics
VITREX SOFT Sterile Blood Lancets
STERILANCE MEDICAL (SUZHOU) INC.
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