BIOTEQUE CORP.

FDA Device Registration & Listing · Taipei, TW · Registration 3012480535

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
3012480535
FEI Number
3012480535
Entity Name
BIOTEQUE CORP.
City/State/Country
Taipei, TW
Establishment Address
5F-6, No.23, Sec.1, Chang-An E. Rd., Taipei 104, TW
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
BIOTEQUE CORP (Owner Number: 9038266)
Owner / Operator Contact Address
5F-6, NO.23, SEC.1, CHANG-AN E. ROAD, TAIPEI, TW-TPE 104, TW
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

TUB500: Tubing, Pump, Infusion line; TUB101: Tubing, Measurement; CATHETERS, SUCTION, TRACHEOBRONCHIAL PACK, HOT OR COLD, DISPOSABLE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KMK Device, Intravascular Catheter Securement General Hospital Class 1 880.5210 2018-07-27
FGE Stents, Drains And Dilators For The Biliary Ducts Gastroenterology, Urology Class 2 876.5010 2025-12-26
LJE Catheter, Nephrostomy Unknown Class U N/A 2025-12-26
GBO Catheter, Nephrostomy, General & Plastic Surgery General, Plastic Surgery Class 1 878.4200 2025-12-26
FEN Device, Cystometric, Hydraulic Gastroenterology, Urology Class 2 876.1620 2011-04-15
FGE Stents, Drains And Dilators For The Biliary Ducts Gastroenterology, Urology Class 2 876.5010 2021-12-20
GBO Catheter, Nephrostomy, General & Plastic Surgery General, Plastic Surgery Class 1 878.4200 2021-12-20
FBK Endoscopic Injection Needle, Gastroenterology-Urology Gastroenterology, Urology Class 2 876.1500 2012-02-21
FBK Endoscopic Injection Needle, Gastroenterology-Urology Gastroenterology, Urology Class 2 876.1500 2026-04-17
BSY Catheters, Suction, Tracheobronchial Anesthesiology Class 1 868.6810 2010-12-28
IMD Pack, Hot Or Cold, Disposable Physical Medicine Class 1 890.5710 2011-07-23

Official Correspondent

WILLIAM LEE

US Agent Details

Ho Shan Wang Email: acmebiotechs@gmail.com Phone: (623) 9864377

Related Public Records

Same Entity

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

Other Registrations for Same Entity

Registration Number Establishment Name Location
3004207966 Bioteque Corporation I-Lan Factory II Su-Ao Cheng Yilan, TW
3035451914 Bioteque Corporation Yilan Science Park Factory Yilan City, TW

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K902734 Olympus Corp. PR CANNULAS 1990-08-22
K880871 John Wagner Associates, Inc. GRABBER WARM PACK/MINI MINI HEATER/FOOT HEATER 1988-05-20

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0008-05 N/A 2
Biliary Stent System (6Fr 9mm x 30mm).
Z-0015-2011 Navilyst Medical, Inc 2
Exodus(TM) 8F (2.7 mm)/25 cm Standard Loop Multipurpose Drainage Catheter with Hydrophilic Coating, REF Catalog No. 10002, UPN Product No. H965100201, Rx ONLY, STERILE/EO --- Made in USA: 2301 Centennial Blvd., Jeffersonville, IN 47130 --- Manufactured for: Navilyst Medical, Inc. 26 Forest Street, Marlborough, MA 01752 USA --- Each box unit contains 5 catheters. --- The Exodus Standard Loop Multipurpose Drainage Catheter consists of a radiopaque polyurethane catheter with a locking pigtail distal end and is coated with a hydrophilic coating. Catheter markings are provided in centimeters on the shaft to indicate the distance form the distal tip. The catheter is provided with a trocar, a metal stiffening cannula and a plastic cannula. Multipurpose Drainage Catheters are intended for percutaneous drainage of fluid in the chest, abdomen and pelvis.
Z-0035-2009 Bard Peripheral Vascular Inc 2
Edwards Lifesciences LifeStent FlexStar Self-Expanding Biliary Stent System, Edwards Lifesciences LLC Irvine, CA 92614, Model EX060201CD. The LifeStent FlexStar self-expanding biliary stent system is intended for use in the palliation of malignant strictures (neoplasms) in the biliary tree.
Z-0036-2009 Bard Peripheral Vascular Inc 2
Edwards Lifesciences LifeStent FlexStar Self-Expanding Biliary Stent System, Edwards Lifesciences LLC Irvine, CA 92614, Model EX060203CD. The LifeStent FlexStar self-expanding biliary stent system is intended for use in the palliation of malignant strictures (neoplasms) in the biliary tree.
Z-0037-2009 Bard Peripheral Vascular Inc 2
Edwards Lifesciences LifeStent FlexStar Self-Expanding Biliary Stent System, Edwards Lifesciences LLC Irvine, CA 92614, Model EX060301CD. The LifeStent FlexStar self-expanding biliary stent system is intended for use in the palliation of malignant strictures (neoplasms) in the biliary tree.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012480535. Last updated year: 2026. Please use registration number 3012480535 when referencing this establishment in official correspondence.
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