KMS Saw Blade 499631309

GUDID 24053613292171

Gebr. Brasseler GmbH & Co. KG

Surgical saw blade, sagittal, single-use

• Primary Device ID: 24053613292171
• NIH Device Record Key: 8f1a1562-eeca-403a-9bd9-c262a3aaedef
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KMS Saw Blade
• Version Model Number: 499631309
• Catalog Number: 499631309
• 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	14053613292174 [Primary]
GS1	24053613292171 [Package]; Contains: 14053613292174; 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 [KMS Saw Blade]

• 24053613292218: 499622210
• 24053613292201: 499629909
• 24053613292195: 499631310
• 24053613292188: 499629910
• 24053613292171: 499631309