GMMI SDN BHD

FDA Device Registration & Listing · IPOH Perak, MY · Registration 3012991986

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3012991986
FEI Number
3012991986
Entity Name
GMMI SDN BHD
City/State/Country
IPOH Perak, MY
Establishment Address
No. 12, Persiaran Industri Rapat 2, Perindustrian Ringan SRI Rapat, IPOH Perak 31350, MY
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
GMMI SDN BHD (Owner Number: 10054920)
Owner / Operator Contact Address
NO 12, Persiaran Industri Rapat 2, Perindustrian Ringan SRI Rapat, IPOH, MY-08 31350, MY
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Stylet - Tracheal Tube/ Bougie Catheter - foldable (CM002) Stylet - Tracheal Tube/ Bougie Catheter (CM001)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BSR Stylet, Tracheal Tube Anesthesiology Class 1 868.5790 2017-05-12

Official Correspondent

No official correspondent registered.

US Agent Details

Amanda Singleton Business: Compliance Systems International, LLC Email: amanda.compliance.sys.intl@gmail.com Phone: (716) 4407364

Related Public Records

Same Entity

GMMI 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 3012991986. Last updated year: 2026. Please use registration number 3012991986 when referencing this establishment in official correspondence.
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