0295724100

GUDID 07613327052961

Hip Cannula, 5.0 mm

STRYKER CORPORATION

Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable

• Primary Device ID: 07613327052961
• NIH Device Record Key: 09e8e327-6076-4dec-b5c0-7c14c2b72166
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 0295724100
• Catalog Number: 0295724100
• Company DUNS: 187502109
• 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: 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(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327052961 [Primary]
GS1	07613327052961 [Primary]
GS1	07613327052961 [Primary]
GS1	07613327052961 [Primary]
GS1	07613327052961 [Primary]
GS1	07613327052961 [Primary]
GS1	07613327052961 [Primary]
GS1	07613327052961 [Primary]
GS1	07613327052961 [Primary]
GS1	07613327052961 [Primary]
GS1	07613327052961 [Primary]
GS1	07613327052961 [Primary]
GS1	07613327052961 [Primary]
GS1	07613327052961 [Primary]

FDA Product Code

• NBH: Accessories, arthroscopic
• NBH: Accessories, arthroscopic
• NBH: Accessories, arthroscopic
• NBH: Accessories, arthroscopic
• NBH: Accessories, arthroscopic
• NBH: Accessories, arthroscopic
• NBH: Accessories, arthroscopic
• NBH: Accessories, arthroscopic
• NBH: Accessories, arthroscopic
• NBH: Accessories, arthroscopic
• NBH: Accessories, arthroscopic
• NBH: Accessories, arthroscopic
• NBH: Accessories, arthroscopic
• NBH: Accessories, arthroscopic

Sterilization

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

[07613327052961]

Moist Heat or Steam Sterilization;Ethylene Oxide

[07613327052961]

Moist Heat or Steam Sterilization;Ethylene Oxide

[07613327052961]

Moist Heat or Steam Sterilization;Ethylene Oxide

[07613327052961]

Moist Heat or Steam Sterilization;Ethylene Oxide

[07613327052961]

Moist Heat or Steam Sterilization;Ethylene Oxide

[07613327052961]

Moist Heat or Steam Sterilization;Ethylene Oxide

[07613327052961]

Moist Heat or Steam Sterilization;Ethylene Oxide

[07613327052961]

Moist Heat or Steam Sterilization;Ethylene Oxide

[07613327052961]

Moist Heat or Steam Sterilization;Ethylene Oxide

[07613327052961]

Moist Heat or Steam Sterilization;Ethylene Oxide

[07613327052961]

Moist Heat or Steam Sterilization;Ethylene Oxide

[07613327052961]

Moist Heat or Steam Sterilization;Ethylene Oxide

[07613327052961]

Moist Heat or Steam Sterilization;Ethylene Oxide

[07613327052961]

Moist Heat or Steam Sterilization;Ethylene Oxide

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-07-31
• Device Publish Date: 2020-07-23

Devices Manufactured by STRYKER CORPORATION

• 03760253800501 - SpineJack: 2020-08-04 PREPARATION KIT 5.0MM
• 03760253800518 - SpineJack: 2020-08-04 PREPARATION KIT 4.2MM
• 03760253800525 - SpineJack: 2020-08-04 PREPARATION KIT 5.8MM
• 33760253800533 - SpineJack: 2020-08-04 INJECTOR TRANSFER TUBE 5.0-5.8MM
• 33760253800540 - SpineJack: 2020-08-04 INJECTOR TRANSFER TUBE 4.2MM
• 33760253800557 - SpineJack: 2020-08-04 CEMENT PUSHER 5.0-5.8MM
• 33760253800564 - SpineJack: 2020-08-04 CEMENT PUSHER 4.2MM
• 07613327053104 - NA: 2020-08-04 Sterilization Tray for Arthroscopy Access Hardware XL