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LAERDAL Pocket Mask - Indonesia BPOM Medical Device Registration

LAERDAL Pocket Mask is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403916283. The device is manufactured by LAERDAL MEDICAL (SUZHOU) CO. LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is IDS MEDICAL SYSTEMS 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 : B
LAERDAL Pocket Mask
Analysis ID: AKL 20403916283

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

IDS MEDICAL SYSTEMS INDONESIA

AR Address

Gedung Wisma 76, Lantai 17 & 22, Jl. LetJend. S. Parman Kav.76, Kelurahan Slipi, Kecamatan Palmerah, 11410

Registration Date

Dec 30, 2024

Expiry Date

Jun 06, 2027

Product Type

Therapeutic Anesthesia Equipment

Nonrebreathing valve.

Non Electromedic Non Sterile

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