4103-260-000S2

GUDID 07613153092735

DHS/DCS Quick Lock Attachment

STRYKER CORPORATION

Surgical drill chuck

• Primary Device ID: 07613153092735
• NIH Device Record Key: ffd65e7b-2be5-446b-842a-2c3e9767aae5
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 4103260000S2
• Catalog Number: 4103-260-000S2
• 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: true
• Serial Number: false
• 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	07613153092735 [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

[07613153092735]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-01-20
• Device Publish Date: 2018-09-24

Devices Manufactured by STRYKER CORPORATION

• 07613327272246 - ARIA: 2025-09-25 IMPLANT IMPACTOR
• 37613327405317 - SurgiCount Safety-Sponge: 2025-09-16 Laparotomy Sponge
• 07613327262209 - XIA: 2025-09-11 FRENCH BENDER
• 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