Bioseal Inc.

Basic Information

• Brand Name: Bioseal Inc.
• Primary DI: 00630094257754
• Version / Model: 25-775B/20
• Company Name: BIOSEAL
• Labeler DUNS: 186968939
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2023-12-26
• Public Version: 1
• Public Version Date: 2024-01-03
• Public Version Status: New
• Public Device Record Key: acf02398-bbde-46ca-b448-a20c626ae600

Device Description

Fletcher Cervix Holding Forceps

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: Yes
• PM Exempt: Yes
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: Yes
• Has Expiration Date: No
• Has Donation ID: No

Sterilization

• Is Sterile: Yes
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
KDC	INSTRUMENT, SURGICAL, DISPOSABLE	General, Plastic Surgery	878.4800	1

GMDN Terms

Code	Name	Definition	Implantable	Status
16469	Manual expandable cervical dilator	A forceps-like surgical instrument designed to manually dilate the cervical canal after its insertion through the cervical os. It is typically constructed with two pivoted handles and opposing blunted blades that expand outward when the handles are manually squeezed, and possibly locked, dilating the cervical canal. This process is used to allow the passage of a curette or other instruments into the uterus. This is a reusable device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Package	10630094257751	GS1	Case	20	In Commercial Distribution
Primary	00630094257754	GS1