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CELOX PPH - Indonesia BPOM Medical Device Registration

CELOX PPH is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603422323. The device is manufactured by MEDTRADE PRODUCTS LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is FA ANTARES MEDIKA.

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
CELOX PPH
Analysis ID: AKL 21603422323

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United Kingdom

Authorized Representative

FA ANTARES MEDIKA

AR Address

RUKO GOLDEN BOULEVARD BLOK I NO.7

Registration Date

Oct 07, 2024

Expiry Date

Feb 13, 2028

Product Type

Surgical Equipment

Nonabsorbable expandable hemostatic sponge for temporary internal use.

Non Electromedic Sterile

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