Scanlan Titanium Bayonet Forceps 3003-840N

GUDID 00846159036282

Scanlan Micro Fcp, fh, bayo sty, 0.3mm curved up, DD tips, 8-3/4"/22 cm

SCANLAN INTERNATIONAL INC

Surgical soft-tissue manipulation forceps, tweezers-like, reusable

• Primary Device ID: 00846159036282
• NIH Device Record Key: 9f6e6d44-7759-4130-a2f7-4c8d8d70b04c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Scanlan Titanium Bayonet Forceps
• Version Model Number: 3003-840N
• Catalog Number: 3003-840N
• Company DUNS: 023055619
• Company Name: SCANLAN INTERNATIONAL INC
• 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: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com
• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00846159036282 [Primary]

FDA Product Code

• GEN: Forceps, General & Plastic Surgery

Sterilization

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

[00846159036282]

Moist Heat or Steam Sterilization

[00846159036282]

Moist Heat or Steam Sterilization

[00846159036282]

Moist Heat or Steam Sterilization

[00846159036282]

Moist Heat or Steam Sterilization

[00846159036282]

Moist Heat or Steam Sterilization

[00846159036282]

Moist Heat or Steam Sterilization

[00846159036282]

Moist Heat or Steam Sterilization

[00846159036282]

Moist Heat or Steam Sterilization

[00846159036282]

Moist Heat or Steam Sterilization

[00846159036282]

Moist Heat or Steam Sterilization

[00846159036282]

Moist Heat or Steam Sterilization

[00846159036282]

Moist Heat or Steam Sterilization

[00846159036282]

Moist Heat or Steam Sterilization

[00846159036282]

Moist Heat or Steam Sterilization

[00846159036282]

Moist Heat or Steam Sterilization

[00846159036282]

Moist Heat or Steam Sterilization

[00846159036282]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-02-10
• Device Publish Date: 2025-01-31

On-Brand Devices [Scanlan Titanium Bayonet Forceps]

• 00846159036282: Scanlan Micro Fcp, fh, bayo sty, 0.3mm curved up, DD tips, 8-3/4"/22 cm
• 00846159012767: Scanlan Micro Fcp, fh, bayo sty, 0.3mm curved up, DD tips, 8-3/4"/22 cm