KM Saw Blade 899624306

GUDID 24053613292300

Gebr. Brasseler GmbH & Co. KG

Surgical saw blade, sagittal, reusable

• Primary Device ID: 24053613292300
• NIH Device Record Key: 8e705228-f11b-4436-a45a-bc71584969d7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KM Saw Blade
• Version Model Number: 899624306
• Catalog Number: 899624306
• Company DUNS: 317409001
• Company Name: Gebr. Brasseler GmbH & Co. KG
• Device Count: 1
• DM Exempt: true
• 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	14053613292303 [Primary]
GS1	24053613292300 [Package]; Contains: 14053613292303; Package: [5 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: 2025-09-08
• Device Publish Date: 2025-08-29

On-Brand Devices [KM Saw Blade]

• 24053613289683: 7000-40SB
• 24053613289690: 7001-40SB
• 24053613292300: 899624306
• 24053613292294: 899623196
• 24053613292287: 899621156
• 24053613292270: 899621196
• 24053613292256: 899621856
• 24053613292249: 899621896
• 24053613292232: 899622556
• 24053613292225: 899622596