KM Saw Blade 7001-40SB

GUDID 24053613289690

Gebr. Brasseler GmbH & Co. KG

Surgical saw blade, sagittal, single-use

• Primary Device ID: 24053613289690
• NIH Device Record Key: 0954d0d2-bdd2-466b-989d-3ee6689f0bb7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KM Saw Blade
• Version Model Number: 7001-40SB
• Catalog Number: 7001-40SB
• Company DUNS: 317409001
• Company Name: Gebr. Brasseler GmbH & Co. KG
• 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	14053613289693 [Primary]
GS1	24053613289690 [Package]; Contains: 14053613289693; Package: [1 Units]; In Commercial Distribution

FDA Product Code

• GFA: Blade, Saw, General & Plastic Surgery, Surgical

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: 2024-07-22
• Device Publish Date: 2024-07-12

On-Brand Devices [KM Saw Blade]

• 24053613289683: 7000-40SB
• 24053613289690: 7001-40SB