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PYFA LW ® Collection Swab Nylon-PP - Indonesia BPOM Medical Device Registration

PYFA LW ® Collection Swab Nylon-PP is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10302220218. The device is manufactured by CITOTEST LABWARE MANUFACTURING CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. PYRIDAM FARMA.

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BPOM Registered
Risk Class Kelas Resiko : A
PYFA LW ® Collection Swab Nylon-PP
Analysis ID: AKL 10302220218

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. PYRIDAM FARMA

AR Address

Sinarmas MSIG Tower Lt. 12 Jl. Jenderal Sudirman Kav. 21 Kelurahan Karet

Registration Date

Dec 10, 2022

Expiry Date

Sep 01, 2024

Product Type

Microbiology Equipment

Microbiological specimen collection and transport device.

Invitro Diagnostics

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