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Official Regulatory Licensure & Quality Compliance
M/S Mehboob Enterprises operates under full statutory compliance with the Drug Regulatory Authority of Pakistan (DRAP), holding Form-4 Licence ELI-EN00000201 for the importation and distribution of medical devices, alongside ISO 13485:2016 and CE compliance.
DRAP Form-4 Medical Device Import Licence
Issued by the Division of Medical Devices & Medicated Cosmetics, Drug Regulatory Authority of Pakistan (DRAP), Ministry of National Health Services, Regulations & Coordination.
Federal Authorization for Medical Device Importation & Distribution
Under Rule 5(2) of the Medical Devices Rules, 2017, the Medical Devices Board (MDB) has officially licensed M/S MEHBOOB ENTERPRISES as an authorized establishment for importing, stocking, and distributing electro-medical and surgical equipment nationwide.
| Licence Number | ELI-EN00000201 |
| Licensing Authority | Drug Regulatory Authority of Pakistan (DRAP) |
| Division | Division of Medical Devices & Medicated Cosmetics |
| MDB Approval Meeting | Meeting No: 131 |
| Licensee Entity | M/S MEHBOOB ENTERPRISES |
| Managing Director (MD) | MEHBOOB ALI (CNIC: 1730119584443) |
| Qualified Incharge Person | AMIR FAYAZ (CNIC: 1710126922581) |
| Authorized Premises | Office No 4, Zaheer Plaza, Latif Abad, Ring Road Peshawar, Khyber Pakhtunkhwa, Pakistan |
| Licence Validity | 10/06/2026 to 09/06/2031 (5-Year Validity) |
| Statutory Scope | Licence to Import Medical Devices (Form-4) |
National & International Quality Accreditations
Every instrument, surgical file, and hospital machine distributed by Mehboob Enterprises conforms to rigorous clinical benchmarks.
DRAP Form-4 Import License
Licence ELI-EN00000201 issued by the Drug Regulatory Authority of Pakistan, granting legal authorization for commercial medical device import and distribution throughout Pakistan.
ISO 13485:2016 Certified QMS
Global Quality Management System compliance specifically mandated for the design, manufacturing, handling, and distribution of precision surgical and medical instruments.
CE Medical Class I & IIa
Conformité Européenne (CE) marking certifying clinical safety, biocompatibility, and metallurgical resistance across all operatory and restorative instrument groups.
NTN & Active Taxpayer Status
Registered with Federal Board of Revenue (FBR) and KP Revenue Authority (KPRA). Fully compliant for government hospital procurement, autonomous institutions, and public tenders.
AISI 420 / 440 Metallurgy
Precision forged from surgical-grade martensitic and austenitic stainless steel alloys, designed to withstand continuous 134°C vacuum autoclave steam cycles without pitting or corrosion.
Manufacturer Direct Warranty
Direct manufacturer accountability on all mechanical forceps, matrix tension rings, and electro-medical units, backed by our local service and inspection center in Peshawar.
Need Certified Documentation for Your Procurement Committee?
We furnish complete tender dossiers—including notarized DRAP Form-4 Import Licences, FBR active taxpayer certificates, ISO 13485 certificates, and manufacturer authorization letters—within 2 hours for procurement boards across Lady Reading Hospital (LRH), Khyber Teaching Hospital (KTH), Hayatabad Medical Complex (HMC), and regional DHQ facilities.
