Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008824562

FEI Number

3008824562

Entity Name

GOLDREIGN PLASTICS (M) SDN BHD

City/State/Country

kajang Selangor, MY

Establishment Address

lot 8,no 23,jalan kesuma 2/1, bandar tasik kesuma, kajang Selangor 43700, MY

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

GOLDREIGN PLASTICS (M0 SDN BHD (Owner Number: 10044659)

Owner / Operator Contact Address

lot 8,no 23,jalan kesuma 2/1, bandar tasik kesuma, kajang, MY-10 43700, MY

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Qlicksmart BladeFLASK

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MMK	Container, Sharps	General Hospital	Class 2	880.5570	2013-07-09

Official Correspondent

kian peng chua

US Agent Details

David Baetens Email: david@oakmedproducts.com Phone: (248) 7620900

Related Public Records

Same Entity

GOLDREIGN PLASTICS (M0 SDN BHD

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008824562. Last updated year: 2026. Please use registration number 3008824562 when referencing this establishment in official correspondence.