Helrex surgical industry
**Kami adalah produsen dan pengekspor instrumen bedah di seluruh dunia.
Helrex Surgical Industry adalah produsen Pakistan yang tepercaya dan pemasok global instrumen bedah, gigi, medis, dan ortopedi berkualitas premium. Dengan komitmen kuat terhadap teknik presisi, standar kualitas internasional, dan keahlian terampil, kami memproduksi rangkaian lengkap gunting bedah, forceps, penahan jarum, retraktor, instrumen tungsten karbida, dan peralatan bedah khusus yang dirancang untuk rumah sakit, klinik, dan profesional kesehatan di seluruh dunia. Setiap instrumen dibuat dengan cermat dari baja tahan karat bermutu tinggi untuk menghasilkan daya tahan, akurasi, ketahanan korosi, dan kinerja klinis yang andal yang luar biasa.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Sialkot, Pakistan
- Founded
- 2019
- Website
- https://helrexsurgical.com
- Categories
- Perlengkapan Medis & Kesehatan
- Markets
- Amerika Serikat, Uni Emirat Arab, Inggris Raya, Austria, Tiongkok, Mesir, Italia, Belanda, Selandia Baru, Pakistan, Qatar, Singapura, Thailand, Suriah, Brasil, Azerbaijan, Australia, Armenia
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- debarment-clear (green), checked 2026-09-03 OpenSanctions
- domain-registered (green), checked 2026-09-03 Domain registry record
- tax-filing-active (green), checked 2026-07-25 FBR Pakistan (ATL Income Tax)
- directors-on-file (green), checked 2026-07-25 FBR Pakistan (IRIS)
- corporate-mail-on-domain (green), checked 2026-09-03 Mail server of the company domain
- web-presence-since (green), checked 2026-09-03 Internet Archive (Wayback)
- blacklist-clear (green), checked 2026-07-25 FBR Pakistan (blacklist)
- contact-email-deliverable (green), checked 2026-07-25
- sanctions-clear (green), checked 2026-09-03 OpenSanctions
Claimed certifications, not confirmed by us
- CE Marking EU NANDO (notified bodies)
- ISO 13485, Medical Devices Quality IAF CertSearch
Import rules for these goods
- 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)
Check independently
Product lines
- Plastic Surgery instruments