APEX Transgulf Manufacturing LLC

FDA Device Registration & Listing · Salalah Z,ufar, OM · Registration 3015173165

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
3015173165
FEI Number
3015173165
Entity Name
APEX Transgulf Manufacturing LLC
City/State/Country
Salalah Z,ufar, OM
Establishment Address
ADH-Plot #1, Warehouse, New Salalah Free Zone, Salalah Z,ufar 211, OM
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
APEX Transgulf Manufacturing LLC (Owner Number: 10087008)
Owner / Operator Contact Address
ADH-Plot #1, Warehouse, New Salalah Free Zone, Salahlah, OM-NOTA 211, OM
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Bag Emisis

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FNY Basin, Emesis General Hospital Class 1 880.6730 2022-12-30

Official Correspondent

No official correspondent registered.

US Agent Details

Rosanna Lee Business: Simcon International LLC Email: rlee@simconintl.com Phone: (847) 9492290

Related Public Records

Same Entity

APEX Transgulf Manufacturing LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015173165. Last updated year: 2026. Please use registration number 3015173165 when referencing this establishment in official correspondence.
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