Helrex surgical industry
**Dünya çapında cerrahi aletler üreticisi ve ihracatçısıyız.
Helrex Surgical Industry, üstün kaliteli cerrahi, dişçilik, tıbbi ve ortopedik aletlerin güvenilir bir Pakistanlı üreticisi ve küresel tedarikçisidir. Hassas mühendisliğe, uluslararası kalite standartlarına ve yetenekli işçiliğe olan güçlü bağlılığımızla, dünya çapındaki hastaneler, klinikler ve sağlık profesyonelleri için tasarlanmış kapsamlı bir cerrahi makas, forseps, iğne tutucu, ekartör, tungsten karbür aletler ve özel cerrahi aletler yelpazesi üretiyoruz. Her alet olağanüstü dayanıklılık, doğruluk, korozyon direnci ve güvenilir klinik performans sunmak için yüksek kaliteli paslanmaz çelikten özenle üretilmiştir.
- 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
- Tıbbi ve Sağlık Malzemeleri
- Markets
- Amerika Birleşik Devletleri, Birleşik Arap Emirlikleri, Birleşik Krallık, Avusturya, Çin, Mısır, İtalya, Hollanda, Yeni Zelanda, Pakistan, Katar, Singapur, Tayland, Suriye, Brezilya, Azerbaycan, Avustralya, Ermenistan
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