7205245

GUDID 00885554008678

MTO KIT XENON XL U.K.

Smith & Nephew, Inc.

Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use Laparoscopic surgical procedure kit, non-medicated, single-use

• Primary Device ID: 00885554008678
• NIH Device Record Key: 2deacbad-0129-49bd-99f9-3fd01b5b96bc
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 7205245
• Catalog Number: 7205245
• Company DUNS: 109903521
• Company Name: Smith & Nephew, Inc.
• 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)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885554008678 [Primary]

FDA Product Code

• FFS: image, illumination, fiberoptic, for endoscope

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: 2020-01-31
• Device Publish Date: 2015-08-23

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• 00885556918623 - R3: 2024-05-23 SZ 42MM BRIDGEBACK REAMER
• 00885556918630 - R3: 2024-05-23 SZ 44MM BRIDGEBACK REAMER
• 00885556918647 - R3: 2024-05-23 SZ 46MM BRIDGEBACK REAMER
• 00885556918654 - R3: 2024-05-23 SZ 48MM BRIDGEBACK REAMER
• 00885556918661 - R3: 2024-05-23 SZ 50MM BRIDGEBACK REAMER
• 00885556918678 - R3: 2024-05-23 SZ 52MM BRIDGEBACK REAMER