TASCO BERHAD

FDA Device Registration & Listing · Port Klang, Selangor, MY · Registration 3032916566

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
3032916566
FEI Number
3032916566
Entity Name
TASCO BERHAD
City/State/Country
Port Klang, Selangor, MY
Establishment Address
Lot 88077, Jalan Perigi Nenas 7/1,, Taman Perindustrian Pulau Indah,, Port Klang, Selangor 42907, MY
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
TASCO Berhad (Owner Number: 10091522)
Owner / Operator Contact Address
Lot 88077, Jalan Perigi Nenas 7/1,, Taman Perindustrian Pulau Indah,, Port Klang,, MY-10 42907, MY
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

LMA Unique Evo Cuff Pilot LMA Unique (Silicone Cuff) Cuff Pilot LMA Supreme LMA Flexible (S) LMA Flexible (SU) LMA Fastrach (SU) LMA Flexible (S) Cuff Pilot LMA Fastrach Stabiliser Rod Cuff Pilot LMA Gastro Cuff Pilot LMA Unique (Silicone Cuff) LMA Protector LMA Classic LMA Supreme Plus Pack LMA Unique Evo LMA Flexible PreCurved Cuff Pilot LMA ProSeal LMA Flexible PreCurved LMA Protector Cuff Pilot

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CAE Airway, Oropharyngeal, Anesthesiology Anesthesiology Class 1 868.5110 2024-10-17

Official Correspondent

Sharonjit Kaur

US Agent Details

Divya Raman Business: Teleflex Inc Email: FDA.US.Agent@Teleflex.Com Phone: (336) 6289038

Related Public Records

Same Entity

TASCO Berhad
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0002-2014 King Systems Corp. 1
King LTS-D Oropharyngeal Airways Product Usage: The King LTS-D is intended for use in adult patients (in excess of 25 kg) for controlled ventilation during anesthesia for procedures that are short in duration and when the patient is considered to have a low risk of aspiration of stomach contents.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3032916566. Last updated year: 2026. Please use registration number 3032916566 when referencing this establishment in official correspondence.
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