HOLLISTER – Adapt Paste - Indonesia BPOM Medical Device Registration

HOLLISTER – Adapt Paste is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10805027503. The device is manufactured by HOLLISTER INCORPORATED, VA from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. LABORA MANDIRI INDO PRATAMA.

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BPOM Registered

Risk Class Kelas Resiko : A

HOLLISTER – Adapt Paste

Analysis ID: AKL 10805027503

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

HOLLISTER INCORPORATED, VA

Country of Origin

United States

Authorized Representative

PT. LABORA MANDIRI INDO PRATAMA

AR Address

Jl. C. Simanjuntak No. 47

Registration Date

Dec 12, 2022

Expiry Date

Dec 31, 2025

Product Type

Therapeutic Gastroenterology-Urology Equipment

Ostomy pouch and accessories.

Non Electromedic Non Sterile

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HOLLISTER – Adapt Paste - Indonesia BPOM Medical Device Registration

Risk Classification

Product Class

Manufacturer

Country of Origin

Authorized Representative

AR Address

Registration Date

Expiry Date

Product Type

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