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KERR Softclamp - Indonesia BPOM Medical Device Registration

KERR Softclamp is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10605220454. The device is manufactured by KERR CORPORATION from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. PURE NOBLE SUN.

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
KERR Softclamp
Analysis ID: AKL 10605220454

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

KERR CORPORATION

Country of Origin

United States

Authorized Representative

PT. PURE NOBLE SUN

AR Address

Jl. Pecenongan No. 82 C Kebon Kelapa, Kec. Gambir Jakarta Pusat 10120

Registration Date

Jan 25, 2023

Expiry Date

Jul 29, 2024

Product Type

Other Dental Equipment

Rubber dam and accessories.

Non Electromedic Non Sterile

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