Wavelink

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Aturan yang berlaku untuk barang ini

Regulasi yang umum berlaku untuk pengiriman di sektor ini. Bukan nasihat hukum: periksa sumber resmi yang ditautkan.

• Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
• For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)
• Electronics for the EU need CE marking incl. RoHS substance limits, and producers must register for WEEE take-back in each member state of sale. European Commission (CE)
• Electronics for the US market need FCC equipment authorization under 47 CFR Part 15, which covers unintentional radiators such as switch-mode power supplies, not only radio devices. US FCC (Part 15)

Kapabilitas distribusi

Peran mitra

Master / Exclusive Distributor

Negara yang dicakup

🇦🇺 Australia 🇳🇿 Selandia Baru

Saluran penjualan

Wholesale & Cash-and-CarryInstitutional & Government Procurement

Jenis pelanggan

Office Suppliers & B2B ProcurementInstitutional & Corporate Buyers

Tentang

Wavelink memutar jaringan nirkabel, handset komunikasi klinis khusus, unit pelacakan seluler, dan rangkaian perangkat lunak kriptografi.

Kategori

Elektronik KonsumenPerlengkapan Medis & Kesehatan

Pasar utama

🇦🇺 Australia 🇳🇿 Selandia Baru

Sertifikasi (dideklarasikan)

ISO 9001, Quality Management

Jelajahi

Distributor di AustraliaElektronik Konsumen di AustraliaPerlengkapan Medis & Kesehatan di Australia