Hudson 4103-135-000

GUDID 04546540216441

1:1 / Modified Trinkle

STRYKER CORPORATION

Drilling power tool attachment, basic

• Primary Device ID: 04546540216441
• NIH Device Record Key: f553f341-96c1-4c5b-b545-7b40f21ab35f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hudson
• Version Model Number: 4103135000
• Catalog Number: 4103-135-000
• Company DUNS: 196548481
• Company Name: STRYKER CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04546540216441 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K972367

FDA Product Code

• KIJ: INSTRUMENT, SURGICAL, ORTHOPEDIC, DC-POWERED MOTOR AND ACCESSORY/ATTACHMENT

Sterilization

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

[04546540216441]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-01-20
• Device Publish Date: 2018-09-24

On-Brand Devices [Hudson]

• 04546540959683: 1:1
• 04546540501684: /Modified Trinkle Attachment
• 04546540501622: Attachment
• 04546540378019: 4:1
• 04546540216526: 4:1 / Modified Trinkle
• 04546540216502: 3.25:1 / Modified Trinkle
• 04546540216489: 3.25:1
• 04546540216441: 1:1 / Modified Trinkle
• 04546540068231: Modified Trinkle Reamer
• 04546540068194: Modified Trinkle Drill