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THERASORB SILVER PLUS - Indonesia BPOM Medical Device Registration

THERASORB SILVER PLUS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603420670. The device is manufactured by WONBIOGEN CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PHARMINDO LESTARI AWARD.

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
THERASORB SILVER PLUS
Analysis ID: AKL 21603420670

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

WONBIOGEN CO., LTD

Country of Origin

Korea

Authorized Representative

PHARMINDO LESTARI AWARD

AR Address

Jl. Boulevard BGR No. 1, Komplek Pergudangan BGR Gudang M, Kel. Kelapa Gading Barat, Kec. Kelapa Gading, Jakarta Utara, DKI Jakarta

Registration Date

Mar 22, 2024

Expiry Date

Jul 03, 2028

Product Type

Surgical Equipment

Hydrophilic wound dressing

Non Electromedic Sterile

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