USB Medical Delivery Foreceps DF-101

GUDID 00853512006790

HV Heart Retractor

NIKOMED USA

Clamp manipulation forceps

• Primary Device ID: 00853512006790
• NIH Device Record Key: 7e45f55f-38d4-43db-a3e5-92c23ae381ba
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: USB Medical Delivery Foreceps
• Version Model Number: DF-101
• Catalog Number: DF-101
• Company DUNS: 073648341
• Company Name: NIKOMED USA
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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

Customer Support Contacts

• Phone: +1(800)355-6456
• Email: info@nikomedusa.com
• Phone: +1(800)355-6456
• Email: info@nikomedusa.com
• Phone: +1(800)355-6456
• Email: info@nikomedusa.com
• Phone: +1(800)355-6456
• Email: info@nikomedusa.com
• Phone: +1(800)355-6456
• Email: info@nikomedusa.com
• Phone: +1(800)355-6456
• Email: info@nikomedusa.com
• Phone: +1(800)355-6456
• Email: info@nikomedusa.com
• Phone: +1(800)355-6456
• Email: info@nikomedusa.com
• Phone: +1(800)355-6456
• Email: info@nikomedusa.com
• Phone: +1(800)355-6456
• Email: info@nikomedusa.com
• Phone: +1(800)355-6456
• Email: info@nikomedusa.com
• Phone: +1(800)355-6456
• Email: info@nikomedusa.com
• Phone: +1(800)355-6456
• Email: info@nikomedusa.com
• Phone: +1(800)355-6456
• Email: info@nikomedusa.com
• Phone: +1(800)355-6456
• Email: info@nikomedusa.com
• Phone: +1(800)355-6456
• Email: info@nikomedusa.com
• Phone: +1(800)355-6456
• Email: info@nikomedusa.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00853512006790 [Primary]

FDA Product Code

• GDJ: Clamp, Surgical, General & Plastic Surgery

Sterilization

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

[00853512006790]

Moist Heat or Steam Sterilization

[00853512006790]

Moist Heat or Steam Sterilization

[00853512006790]

Moist Heat or Steam Sterilization

[00853512006790]

Moist Heat or Steam Sterilization

[00853512006790]

Moist Heat or Steam Sterilization

[00853512006790]

Moist Heat or Steam Sterilization

[00853512006790]

Moist Heat or Steam Sterilization

[00853512006790]

Moist Heat or Steam Sterilization

[00853512006790]

Moist Heat or Steam Sterilization

[00853512006790]

Moist Heat or Steam Sterilization

[00853512006790]

Moist Heat or Steam Sterilization

[00853512006790]

Moist Heat or Steam Sterilization

[00853512006790]

Moist Heat or Steam Sterilization

[00853512006790]

Moist Heat or Steam Sterilization

[00853512006790]

Moist Heat or Steam Sterilization

[00853512006790]

Moist Heat or Steam Sterilization

[00853512006790]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-03-21
• Device Publish Date: 2023-03-13

Devices Manufactured by NIKOMED USA

• 20853512006954 - NIKOTRACE: 2025-08-18 ECG Electrodes
• 20853512006961 - NIKOTRACE: 2025-08-18 Repositionable ECG Electrodes
• 30853512006517 - NikoSurg: 2025-06-18 Neutral Electrodes
• 20853512006572 - NikoSurg: 2025-06-18 Neutral Electrodes
• 20853512006817 - NIKOTRACE: 2025-03-31 ECG Electrodes
• 00853512006820 - NIKOTRACE: 2025-03-31 ECG Electrodes
• 20853512006831 - NIKOTRACE: 2025-03-31 ECG Electrodes
• 20853512006848 - NIKOTRACE: 2025-03-31 ECG Electrodes