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MOYUUM Silicone Teether - Indonesia BPOM Medical Device Registration

MOYUUM Silicone Teether is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10604420099. The device is manufactured by SHINSUNG SILICONE CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. TIGASATU MEDIKA SOLUSINDO.

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.

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BPOM Registered
Risk Class Kelas Resiko : A
MOYUUM Silicone Teether
Analysis ID: AKL 10604420099

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Korea

Authorized Representative

PT. TIGASATU MEDIKA SOLUSINDO

AR Address

Karawaci Office Park, Jalan Imam Bonjol, Ruko Finangsia Blok H 53, Prov. Banten, Kota Tangerang, Kec. Cibodas, Kel. Panunggangan Barat

Registration Date

Oct 25, 2024

Expiry Date

Jun 24, 2029

Product Type

Therapeutic Dental Equipment

Teething ring.

Non Electromedic Non Sterile

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