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FEMTO LDV - Indonesia BPOM Medical Device Registration

FEMTO LDV is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203516233. The device is manufactured by WG SURGICAL INSTRUMENT ENGINEERING from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRIASTRI MEDITAMA.

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 : C
FEMTO LDV
Analysis ID: AKL 21203516233

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Switzerland

Authorized Representative

PT. TRIASTRI MEDITAMA

AR Address

JL. INDUSTRI NO.9-11 GUNUNG SAHARI UTARA,

Registration Date

Jun 16, 2023

Expiry Date

May 08, 2028

Product Type

Surgical Eye Equipment

Ophthalmic laser.

Electromedic Radiation

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