DBK9CC

GUDID 07613327169379

STRYKER CORPORATION

External cuff/pad connection tubing

• Primary Device ID: 07613327169379
• NIH Device Record Key: ae25d5d6-de16-409a-8f67-9e4ab88c4010
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: DBK9CC
• Catalog Number: DBK9CC
• Company DUNS: 078470558
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327169379 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K100585

FDA Product Code

• DWJ: System, thermal regulating

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-03-21
• Device Publish Date: 2016-09-24

Devices Manufactured by STRYKER CORPORATION

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• 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
• 07613327262438 - XIA: 2025-09-11 AWL