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DELPHI Vaginal Self Sampler - Indonesia BPOM Medical Device Registration

DELPHI Vaginal Self Sampler is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203220111. The device is manufactured by ZMC TECHNOLOGIES PTE., LTD. from Singapore, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. UBC MEDICAL INDONESIA.

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 : A
DELPHI Vaginal Self Sampler
Analysis ID: AKL 10203220111

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Singapore

Authorized Representative

PT. UBC MEDICAL INDONESIA

AR Address

Jalan Rawa Gelam V, Blok L Kav. 11-13, Kawasan Industri Pulogadung Jakarta Timur13930

Registration Date

Sep 29, 2022

Expiry Date

Jun 01, 2027

Product Type

Pathology Equipment and Accessories

Specimen transport and storage container.

Invitro Diagnostics

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