Kevorkian Biopsy Punch 030103

GUDID M803030103

Kevorkian Biopsy Punch 81/2" (216mm)

MEDGYN PRODUCTS, INC.

Intrauterine curette, manual

• Primary Device ID: M803030103
• NIH Device Record Key: 05215cac-e3f0-4557-90e6-77a674de44d7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Kevorkian Biopsy Punch
• Version Model Number: Kevorkian Biopsy Punch 81/2" (216mm)
• Catalog Number: 030103
• 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	M803030103 [Primary]

FDA Product Code

• KOH: Instrument, Manual, General Obstetric-Gynecologic

Sterilization

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

[M803030103]

Moist Heat or Steam Sterilization

[M803030103]

Moist Heat or Steam Sterilization

[M803030103]

Moist Heat or Steam Sterilization

[M803030103]

Moist Heat or Steam Sterilization

[M803030103]

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]

• M80303010310: Kevorkian Biopsy Punch 10" (254mm)
• M803030103: Kevorkian Biopsy Punch 81/2" (216mm)