Kevorkian Biopsy Punch Gold Titanium 030187

GUDID M803030187

Kevorkian Biopsy Punch Gold Titanium (200mm)

MEDGYN PRODUCTS, INC.

Intrauterine curette, manual

• Primary Device ID: M803030187
• NIH Device Record Key: 1c2b121b-17e3-48e5-adbf-82cae72b2f26
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Kevorkian Biopsy Punch Gold Titanium
• Version Model Number: Kevorkian Biopsy Punch Gold Titanium (200mm)
• Catalog Number: 030187
• 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	M803030187 [Primary]

FDA Product Code

• KOH: Instrument, Manual, General Obstetric-Gynecologic

Sterilization

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

[M803030187]

Moist Heat or Steam Sterilization

[M803030187]

Moist Heat or Steam Sterilization

[M803030187]

Moist Heat or Steam Sterilization

[M803030187]

Moist Heat or Steam Sterilization

[M803030187]

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 Gold Titanium ]

• M803030187: Kevorkian Biopsy Punch Gold Titanium (200mm)
• M803030186: Kevorkian Biopsy Punch Gold Titanium (250mm)