A-Silicone for Bite Registration - Indonesia BPOM Medical Device Registration
A-Silicone for Bite Registration is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602420039. The device is manufactured by SHANDONG HUGE DENTAL MATERIAL CORPORATION from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is QUALTEK CONSULTANT JAKARTA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHANDONG HUGE DENTAL MATERIAL CORPORATIONCountry of Origin
China
Authorized Representative
QUALTEK CONSULTANT JAKARTAAR Address
Icon Business Park Blok K No 6, BSD City, Kab Tangerang, Banten
Registration Date
Jan 29, 2024
Expiry Date
Oct 09, 2028
Product Type
Prosthetic Dental Equipment
Impression material.
Non Electromedic Non Sterile
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GumEasy Duplication Silicone Material
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PEGAVISION Daily Disposable Soft Contact Lenses
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SIGMA Sterilization Pouch
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CLINY PTCD Kit
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CLINY Self-Catheterization Set
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CLINY Nephrostomy Kit
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AiBS-01
FUTURE INC.

