Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011947913

FEI Number

3011947913

Entity Name

BACH VIET PLASTIC

City/State/Country

Ho Chi Minh city, VN

Establishment Address

42 Huynh Thi Phung Street, 4th Ward, District 8, Ho Chi Minh city 5427, VN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Omnicell Global (Owner Number: 10052459)

Owner / Operator Contact Address

6600 Transcanada Hwy suite 206, Montreal, CA-QC H9R 4S2, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Specimen Container Histocell Cassettes Inoculation Loop

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NNK	Container, Specimen Mailer And Storage, Non-Sterile	Pathology	Class 1	864.3250	2016-08-01
IDZ	Cassettes, Tissue	Pathology	Class 1	864.3010	2016-08-01
LIB	Device, General Purpose, Microbiology, Diagnostic	Microbiology	Class 1	866.2660	2016-08-01

Official Correspondent

Eric Truong

US Agent Details

Dennis Hoeft Business: Globe Scientific. Inc. Email: D.Hoeft@globescientific.com Phone: (201) 5991400

Related Public Records

Same Entity

Omnicell Global

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011947913. Last updated year: 2026. Please use registration number 3011947913 when referencing this establishment in official correspondence.