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COLLACONE - Indonesia BPOM Medical Device Registration

COLLACONE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31603324912. The device is manufactured by BOTISS BIOMATERIALS GMBH from Germany, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. GRATIA JAYA MULYA.

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
COLLACONE
Analysis ID: AKL 31603324912

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Germany

Authorized Representative

PT. GRATIA JAYA MULYA

AR Address

Gading Park View, Jl. Boulevard Timur Raya Blok ZC I No. 10-11, RT.4/RW.11, Kel. Kelapa Gading Timur, Kec. Kelapa Gading, Kota Adm. Jakarta Utara, Provinsi DKI Jakarta, Kode Pos 14250

Registration Date

Sep 07, 2023

Expiry Date

Feb 15, 2028

Product Type

Surgical Equipment

Absorbable hemostatic agent and dressing.

Non Electromedic Sterile

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