BOVIE® H10012

GUDID 10607151012172

H-TYPE SHARP TIP DISPOSABLE DERMAL ELECTRODE, NON-STERILE

ASPEN SURGICAL PRODUCTS, INC.

Open-surgery electrosurgical electrode, monopolar, single-use

• Primary Device ID: 10607151012172
• NIH Device Record Key: e42b1eed-a5b7-4a06-b81c-9123588d644c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BOVIE®
• Version Model Number: H10012
• Catalog Number: H10012
• Company DUNS: 027680821
• Company Name: ASPEN SURGICAL PRODUCTS, INC.
• Device Count: 100
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• 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
GS1	00607151012175 [Unit of Use]
GS1	10607151012172 [Primary]

FDA Product Code

• HGI: Electrocautery, Gynecologic (And Accessories)

Sterilization

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

[10607151012172]

Ethylene Oxide

[10607151012172]

Ethylene Oxide

[10607151012172]

Ethylene Oxide

[10607151012172]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2025-12-30
• Device Publish Date: 2017-06-15

On-Brand Devices [BOVIE®]

• 10607151012189: H-TYPE BLUNT TIP DISPOSABLE DERMAL ELECTRODE, NON-STERILE
• 10607151012172: H-TYPE SHARP TIP DISPOSABLE DERMAL ELECTRODE, NON-STERILE