DDM Pneumatic Tourniquet - Indonesia BPOM Medical Device Registration
DDM Pneumatic Tourniquet is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21604520004. The device is manufactured by SPENGLER SAS. from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. USAHA PUTRASEJATI SUKSES.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SPENGLER SAS.Country of Origin
France
Authorized Representative
PT. USAHA PUTRASEJATI SUKSESAR Address
Rukan Crown Blok A No 35 Green Lake City
Registration Date
Jan 30, 2025
Expiry Date
Aug 19, 2029
Product Type
Therapeutic Surgical Equipment
Pneumatic tourniquet.
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