Kevorkian Biopsy Punch Titanium 030126

GUDID M803030126

Kevorkian Biopsy Punch Titanium 8.5" (216mm)

MEDGYN PRODUCTS, INC.

Intrauterine curette, manual

• Primary Device ID: M803030126
• NIH Device Record Key: 95f574e4-0083-40c3-a150-a62e3b858ad9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Kevorkian Biopsy Punch Titanium
• Version Model Number: Kevorkian Biopsy Punch Titanium 8.5" (216mm)
• Catalog Number: 030126
• Company DUNS: 103913430
• Company Name: MEDGYN PRODUCTS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M803030126 [Primary]

FDA Product Code

• KOH: Instrument, Manual, General Obstetric-Gynecologic

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[M803030126]

Moist Heat or Steam Sterilization

[M803030126]

Moist Heat or Steam Sterilization

[M803030126]

Moist Heat or Steam Sterilization

[M803030126]

Moist Heat or Steam Sterilization

[M803030126]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-11-24
• Device Publish Date: 2025-11-16

On-Brand Devices [Kevorkian Biopsy Punch Titanium ]

• M803030174: Kevorkian Biopsy Punch Titanium 10" (254mm) Heavy Grip Handle
• M803030126: Kevorkian Biopsy Punch Titanium 8.5" (216mm)