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VIDA PDO - Indonesia BPOM Medical Device Registration

VIDA PDO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603222805. The device is manufactured by FOOSIN MEDICAL SUPPLIER INC., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. DANVI MEDILAB PERKASA.

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 : C
VIDA PDO
Analysis ID: AKL 21603222805

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. DANVI MEDILAB PERKASA

AR Address

Jl. Kapten Muslim Komp. Mega Com Center Blok G No. 1-2 Kel. Dwikora Kec. Medan Helvetia

Registration Date

Nov 21, 2023

Expiry Date

Nov 28, 2025

Product Type

Surgical Equipment

Absorbable polydioxanone surgical suture.

Non Electromedic Sterile

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