ADP10CE

GUDID 07613327277708

STRYKER CORPORATION

Electrical-only medical device connection cable, reusable

• Primary Device ID: 07613327277708
• NIH Device Record Key: 8421317c-09df-4a97-a764-b24f4af0caed
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: ADP10CE
• Catalog Number: ADP10CE
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327277708 [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: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-24

Devices Manufactured by STRYKER CORPORATION

• 37613327548205 - Neptune SafeAir: 2025-01-14 Telescopic Smoke Evacuation Pencil, Push Button, Coated, No PVC
• 07613327273120 - TRIO: 2025-01-03 PEDICULAR SCREWDRIVER SHAFT
• 07613327273144 - TRIO +: 2025-01-03 SELF HOLDING PEDICULAR SCREWDRIVER
• 07613327273175 - TRIO +: 2025-01-03 FLEXIBLE EXTENDER III
• 07613327273182 - TRIO: 2025-01-03 ROD BENDER
• 07613327273205 - TRIO: 2025-01-03 SPONDYLOSISTHESIS REDUCTION INSTRUMENT
• 07613327273212 - TRIO: 2025-01-03 SPONDYLOLISTHESIS REDUCTION INSTRUMENT
• 07613327273243 - TRIO +: 2025-01-03 FLEXIBLE EXTENDER II