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PROSTROLANE NATURAL_B - Indonesia BPOM Medical Device Registration

PROSTROLANE NATURAL_B is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602917336. The device is manufactured by CAREGEN CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is HERCA CIPTA DERMAL PERDANA.

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 : D
PROSTROLANE NATURAL_B
Analysis ID: AKL 31602917336

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

CAREGEN CO., LTD

Country of Origin

Korea

Authorized Representative

HERCA CIPTA DERMAL PERDANA

AR Address

Taman Harapan Indah Blok FF 1 B No. 10 Kel. Jelambar Baru, Kec. Grogol Petamburan Jakarta Barat 11460

Registration Date

Sep 08, 2022

Expiry Date

Jul 07, 2027

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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