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REVMEDX Injectable Hemostatic Device - Indonesia BPOM Medical Device Registration

REVMEDX Injectable Hemostatic Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603222421. The device is manufactured by REVMEDX, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. RANAYA FAZZA UTAMA.

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BPOM Registered
Risk Class Kelas Resiko : B
REVMEDX Injectable Hemostatic Device
Analysis ID: AKL 21603222421

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

REVMEDX, INC.

Country of Origin

United States

Authorized Representative

PT. RANAYA FAZZA UTAMA

AR Address

Graha Harapan Blok E14/12

Registration Date

Oct 10, 2022

Expiry Date

Sep 22, 2026

Product Type

Surgical Equipment

Nonabsorbable expandable hemostatic sponge for temporary internal use.

Non Electromedic Non Sterile

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