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SLOCK Fixture - Indonesia BPOM Medical Device Registration

SLOCK Fixture is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602420159. The device is manufactured by KOREA DENTAL IMPLANT, INC. (KDI, INC.) from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. NHM MEDITECH INDONESIA.

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 : C
SLOCK Fixture
Analysis ID: AKL 20602420159

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

PT. NHM MEDITECH INDONESIA

AR Address

JALAN PITANIAGA NOMOR 6 LANTAI 1 RT.001 RW.011 KEL CIEPEUNDEUY KEC PADALARANG KAB.BANDUNG BARAT KODE 40553

Registration Date

Mar 27, 2024

Expiry Date

Jan 16, 2029

Product Type

Prosthetic Dental Equipment

Endosseous dental implant

Non Electromedic Sterile

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