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Seal it - Indonesia BPOM Medical Device Registration

Seal it is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602220290. The device is manufactured by SPIDENT CO.,LTD from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MITRA HARAPAN MANDIRI.

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BPOM Registered
Risk Class Kelas Resiko : B
Seal it
Analysis ID: AKL 20602220290

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

SPIDENT CO.,LTD

Country of Origin

Korea

Authorized Representative

PT. MITRA HARAPAN MANDIRI

AR Address

The Bellezza Shopping Arcade 2nd Floor Unit 69-71 Jl. Letjen Soepeno No 34 Arteri Permata Hijau, Jakarta 12210 Indonesia

Registration Date

Oct 24, 2022

Expiry Date

Dec 31, 2026

Product Type

Prosthetic Dental Equipment

Pit and fissure sealant and conditioner.

Non Electromedic Non Sterile

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