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DDM Pneumatic Tourniquet - Indonesia BPOM Medical Device Registration

DDM Pneumatic Tourniquet is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21604520004. The device is manufactured by SPENGLER SAS. from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. USAHA PUTRASEJATI SUKSES.

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BPOM Registered
Risk Class Kelas Resiko : B
DDM Pneumatic Tourniquet
Analysis ID: AKL 21604520004

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

SPENGLER SAS.

Country of Origin

France

Authorized Representative

PT. USAHA PUTRASEJATI SUKSES

AR Address

Rukan Crown Blok A No 35 Green Lake City

Registration Date

Jan 30, 2025

Expiry Date

Aug 19, 2029

Product Type

Therapeutic Surgical Equipment

Pneumatic tourniquet.

Non Radiation Electromedics

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