Data / Medical devices / Taiwan / Pacific Hospital Supply Co. Ltd.

Pacific Hospital Supply Co. Ltd.: FDA-registered device maker in Taipei, Taiwan, 4 510(k) clearances

Name: Pacific Hospital Supply Co. Ltd. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Pacific Hospital Supply Co. Ltd. is registered with the FDA (registration 8044099) in Taipei, Taiwan. It lists 17 device types. The FDA files 4 510(k) clearances under its listings, the newest dated August 27, 2024. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 8044099
FEI number: 3004458261
Address: 4 F., No. 160, Daye Road Beitou District, Taipei, Taiwan, 112
Owner or operator: PACIFIC HOSPITAL SUPPLY CO. LTD. (9005460)
Roles: Exporter to the US
First device listed: August 16, 1995
Registered through: 2026
Brand names listed: urine meter

Devices it lists

Device	Product code	Class	Role	Source
Accessories, Catheter	KGZ	1	Exporter to the US	accessdata.fda.gov
Airway, Nasopharyngeal	BTQ	1	Exporter to the US	accessdata.fda.gov
Bottle, Collection, Vacuum	KDQ	2	Exporter to the US	accessdata.fda.gov
Cannula, Suction, Uterine	HGH	2	Exporter to the US	accessdata.fda.gov
Catheter And Tip, Suction	JOL	2	Exporter to the US	accessdata.fda.gov
Catheters, Suction, Tracheobronchial	BSY	1	Exporter to the US	accessdata.fda.gov
Circuit, Breathing (W Connector, Adaptor, Y Piece)	CAI	1	Exporter to the US	accessdata.fda.gov
Collector, Urine, (And Accessories) For Indwelling Catheter	KNX	2	Exporter to the US	accessdata.fda.gov
Curette, Suction, Endometrial (And Accessories)	HHK	2	Exporter to the US	accessdata.fda.gov
Dilator, Cervical, Fixed Size	HDQ	1	Exporter to the US	accessdata.fda.gov
Gastrointestinal Tubes With Enteral Specific Connectors	PIF	2	Exporter to the US	accessdata.fda.gov
Humidifier, Non-Direct Patient Interface (Home-Use)	KFZ	1	Exporter to the US	accessdata.fda.gov
Injector And Syringe, Angiographic	DXT	2	Exporter to the US	accessdata.fda.gov
Kit, Surgical Instrument, Disposable	KDD	1	Exporter to the US	accessdata.fda.gov
Sterilization Wrap Containers, Trays, Cassettes & Other Accessories	KCT	2	Exporter to the US	accessdata.fda.gov
System, Abortion, Vacuum	HHI	2	Exporter to the US	accessdata.fda.gov
Tubing, Noninvasive	GAZ	2	Exporter to the US	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
August 27, 2024	K242212	Disposable Syringe (Kit); Nemoto Disposable Syringe (Kit)	DXT	Substantially Equivalent	Nemoto Kyorindo Co., Ltd.	accessdata.fda.gov
October 1, 2020	K202357	Nutricare Clear-ISOSAF Nasogastric Feeding Tube	PIF	Substantially Equivalent	Three Circles Consulting Limited	accessdata.fda.gov
April 5, 2016	K151503	NUTRICARE-ISOSAF NASO-GASTRIC FEEDING TUBE	PIF	Substantially Equivalent	Gbuk Enteral Limited	accessdata.fda.gov
April 14, 1977	K770590	SURGI-KIT	KCT	Substantially Equivalent	Ethox Corp.	accessdata.fda.gov

Compare with other makers

Updated August 27, 2024. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.