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TURTLEPIN®III 2.0 (7) - Indonesia BPOM Medical Device Registration

TURTLEPIN®III 2.0 (7) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603220008. The device is manufactured by JMBIOTECH CORPORATION LIMITED from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PYRIDAM FARMA.

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 : B
TURTLEPIN®III 2.0 (7)
Analysis ID: AKL 21603220008

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

PT. PYRIDAM FARMA

AR Address

Sinarmas MSIG Tower Lt. 12 Jl. Jenderal Sudirman Kav. 21 Kelurahan Karet

Registration Date

Jan 03, 2022

Expiry Date

Sep 29, 2026

Product Type

Surgical Equipment

Microneedling Device for Aesthetic Use

Non Electromedic Sterile

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