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PIGEON Teether Step 1 - Indonesia BPOM Medical Device Registration

PIGEON Teether Step 1 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10604812317. The device is manufactured by PIGEON INDUSTRIES THAILAND from Thailand, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MULTI INDOCITRA. TBK.

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
PIGEON Teether Step 1
Analysis ID: AKL 10604812317

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Thailand

Authorized Representative

PT. MULTI INDOCITRA. TBK

AR Address

Green Central City, Commercial Area Lantai 6 Jl Gajah Mada No.188, Jakarta 11120

Registration Date

Mar 31, 2022

Expiry Date

Sep 20, 2026

Product Type

Therapeutic Dental Equipment

Teething ring.

Non Electromedic Non Sterile

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