5300010943

GUDID 07613153000723

7.0mm Straight Dermabrader Medium

STRYKER CORPORATION

Dermatome blade, single-use

• Primary Device ID: 07613153000723
• NIH Device Record Key: 3b9dd5ed-06c3-4ac0-92f9-bbaf462ec1ac
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 5300010943
• Catalog Number: 5300010943
• Company DUNS: 196548481
• Company Name: STRYKER CORPORATION
• 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: false
• 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

Customer Support Contacts

• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
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Device Dimensions

• Length: 49 Millimeter
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Device Identifiers

Device Issuing Agency	Device ID
GS1	07613153000723 [Primary]

FDA Product Code

• GFE: BRUSH, DERMABRASION, POWERED

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: 2018-10-24
• Device Publish Date: 2018-09-23

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• 07613327262216 - XIA: 2025-09-11 SPREADER
• 07613327262254 - XIA: 2025-09-11 COMPRESSOR
• 07613327262261 - XIA: 2025-09-11 BLUNT PROBE
• 07613327262292 - XIA: 2025-09-11 TORQUE WRENCH
• 07613327262414 - XIA: 2025-09-11 STANDARD T-HANDLE