Susol® Forceps Artery Halstead Mosquito Straight 12.5cm

GUDID 05060418834128

BAILEY INSTRUMENTS LTD

Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use

• Primary Device ID: 05060418834128
• NIH Device Record Key: 3df9caaf-49fb-4ecb-9903-11d74b014e0a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Susol® Forceps Artery Halstead Mosquito Straight 12.5cm
• Version Model Number: SS09-0625
• Company DUNS: 769260357
• Company Name: BAILEY INSTRUMENTS LTD
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• 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	05060418832803 [Package]; Package: Pack [10 Units]; In Commercial Distribution
GS1	05060418834128 [Primary]

FDA Product Code

• GEN: Forceps, General & Plastic Surgery

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-01-31
• Device Publish Date: 2024-01-23

Devices Manufactured by BAILEY INSTRUMENTS LTD

• 05060418833671 - Susol® Emery Board 18cm: 2024-03-06
• 05060418832377 - Susol® Diamond Bur Pear 2: 2024-03-06
• 05060418832407 - Susol® Diamond Bur Pear 1: 2024-03-06
• 05060418832414 - Susol® Diamond Bur 15C: 2024-03-06
• 05060418832421 - Susol® Diamond Bur 1HP Enucleator: 2024-03-06
• 05060418832674 - Susol® Blacks File SE Standard 14cm: 2024-03-06
• 05060418832698 - Susol® Probe Flat Head Swan Neck 12.5cm: 2024-03-06
• 05060418832704 - Susol® Blacks File Double Ended Micro with Round Probe 14cm: 2024-03-06