Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030178466

FEI Number

3030178466

Entity Name

MIDA PRECISION MOLD CORPORATION

City/State/Country

My Yen Commune Tay Ninh, VN

Establishment Address

Highway 1A, Hamlet 1, My Yen Commune Tay Ninh 80000, VN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

MIDA Precision Mold Corporation (Owner Number: 10089187)

Owner / Operator Contact Address

Highway 1A, Hamlet 1, My Yen Commune, VN-37 80000, VN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Microcentrifuge tube 2ml Microcentrifuge tube 0.2ml Microcentrifuge tube 1.5ml 15ml Screw Cap Centrifuge Tube 50ml Screw Cap Centrifuge Tube 15ml Snap Cap Centrifuge Tube 50ml Snap Cap Centrifuge Tube Self Stand 50ml Snap Cap Centrifuge Tube Self Stand 50ml Screw Cap Centrifuge Tube Yellow Pipette Tip 200ul Inner Test Tube Cap ø16 8-Strip PCR Tube 0.2ml Outer Test Tube Cap Vacuum Test Tube Cap - K1 Double color rubber cap 8-Strip PCR Tube 0.15ml Vacuum Test Tube Cap - K2 Inner Test Tube Cap ø12 Blue Pipette Tip 1000ul Stick/Loop 10ul Stick/Loop 1ul Pill Organizer Baby Nose Cleaner 10015 Square Petri Dish 9015 Petri Dish 10025 Petri Dish 9015 - 2 Sections Petri Dish 9015 - 3 Sections Petri Dish 9014 Petri Dish 509 Petri Dish 6515 Petri Dish 6015 Petri Dish Fireless Therapy Cupping Pill crusher

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JQC	Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use	Clinical Chemistry	Class 1	862.2050	2023-11-14
LXG	Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use	Clinical Chemistry	Class 1	862.2050	2023-11-14
LIB	Device, General Purpose, Microbiology, Diagnostic	Microbiology	Class 1	866.2660	2023-11-14
NXB	Dispenser, Solid Medication	Physical Medicine	Class 1	890.5050	2023-11-14
KYZ	Syringe, Irrigating (Non Dental)	General Hospital	Class 1	880.6960	2023-11-14
KIZ	Dish, Tissue Culture	Hematology	Class 1	864.2240	2023-11-14
KNM	Device, Pressure Applying	Physical Medicine	Class 1	890.5765	2024-01-12
OHY	Pill Crusher/Cutter	General Hospital	Class 1	880.6430	2023-11-14

Official Correspondent

Nguyen Chuc

US Agent Details

Oliver Farnsworth Richard William Business: GLOBAL INSPECTION AND CERTIFICATION NETWORK (CGLOBAL) CORP Email: Oski30@icloud.com Phone: (716) 4034085

Related Public Records

Same Entity

MIDA Precision Mold Corporation

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K944481	Garan Scientific, Inc.	THE HEART PROTECTOR	1995-04-10

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0002-2008	Beckman Coulter Inc	1	FP1000 Cell Preparation System Software versions 1.1 & 1.2, Part Number 624922, for in vitro diagnostic use.
Z-0023-2013	Biomerieux Inc	1	PREVI Isola System, Catalog numbers 29500 and 29500R, bioMerieux, Inc., Durham, NC. Intended to perform the inoculation and streaking of Prepoured Media (PPM) with liquid microbiological samples.

Similar Registrations

Registration Number	Establishment Name	Location
3010394461	HERMLE LABORTECHNIK GMBH	Wehingen Baden-Wurttemberg, DE
3004198394	BECKMAN COULTER, INC.	INDIANAPOLIS, IN, US
3033848228	JOAN LAB EQUIPMENT (ZHEJIANG) CO.,LTD.	Huzhou Zhejiang, CN
3004142400	GLOBUS MEDICAL, INC.	AUDUBON, PA, US
3017155466	KIT COMPANY	Phoenix, AZ, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030178466. Last updated year: 2026. Please use registration number 3030178466 when referencing this establishment in official correspondence.