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ENDOPATH Ultra Veress Insufflation Needles - Indonesia BPOM Medical Device Registration

ENDOPATH Ultra Veress Insufflation Needles is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21106320086. The device is manufactured by HARMAC MEDICAL PRODUCTS, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. JOHNSON AND JOHNSON INDONESIA TWO.

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BPOM Registered
Risk Class Kelas Resiko : B
ENDOPATH Ultra Veress Insufflation Needles
Analysis ID: AKL 21106320086

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. JOHNSON AND JOHNSON INDONESIA TWO

AR Address

Revenue Tower, Lt.27 District 8, SCBD Lot 13 Jl. Jenderal Sudirman Kav. 52-53 Jakarta 12190, Indonesia

Registration Date

Jan 12, 2025

Expiry Date

Jan 26, 2028

Product Type

Diagnostic Obstetric and Gynaecological Equipment

Laparoscopic insufflator.

Non Electromedic Sterile

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