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DR. HONLE DERMALIGHT® 80 - Indonesia BPOM Medical Device Registration

DR. HONLE DERMALIGHT® 80 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603716197. The device is manufactured by DR. K. HONLE MEDIZINTECHNIK. LTD. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. 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 : B
DR. HONLE DERMALIGHT® 80
Analysis ID: AKL 21603716197

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. 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

May 15, 2023

Expiry Date

Feb 15, 2028

Product Type

Surgical Equipment

Ultraviolet lamp for dermatologic disorders.

Non Radiation Electromedics

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