PathTezt®

Basic Information

• Brand Name: PathTezt®
• Primary DI: 09551020410252
• Version / Model: PCS-200901
• Company Name: BIOCYTECH CORPORATION SDN. BHD.
• Labeler DUNS: 865773902
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2026-03-11
• Public Version: 1
• Public Version Date: 2026-03-19
• Public Version Status: New
• Public Device Record Key: 6801d0d8-c21f-44dd-bb2a-cd267139e349

Device Description

Preservation and transportation of cell material from the vagina.

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): No
• Over the Counter (OTC): No
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: No
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: No
• PM Exempt: Yes
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: Yes
• Has Expiration Date: Yes
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
LEA	Preservative, Cytological	Pathology	864.4010	1

GMDN Terms

Code	Name	Definition	Implantable	Status
57952	Cytology specimen container IVD, transport buffer	A covered receptacle containing transport buffer solution intended to be used for the collection, preservation, and transport of a cytology specimen (e.g., oral, cervical, colonic) for in vitro diagnostic investigation [e.g., histopathological cervical cancer screening]. It does not contain patient-contact specimen sampling/extraction devices such as swabs/brushes. This is a single-use device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	09551020410252	GS1