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VIDA Connecting Tube with or without Yankauer Handle - Indonesia BPOM Medical Device Registration

VIDA Connecting Tube with or without Yankauer Handle is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902420815. The device is manufactured by WELL LEAD MEDICAL CO.,LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. DANVI MEDILAB PERKASA.

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BPOM Registered
Risk Class Kelas Resiko : C
VIDA Connecting Tube with or without Yankauer Handle
Analysis ID: AKL 20902420815

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 22, 2024

Expiry Date

Aug 05, 2027

Product Type

Therapeutic General and Individual Hospital Equipment

Intravascular administration set.

Non Electromedic Sterile

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