DOUBLE PUMP RF 72204055

GUDID 00885554037548

DOUBLE PUMP RF PATIENT CASSETTE 20/BX

Smith & Nephew, Inc.

Arthroscopic irrigation/insufflation system

• Primary Device ID: 00885554037548
• NIH Device Record Key: e4d0dcde-63a4-46e5-85fd-c4d228412acc
• Commercial Distribution Discontinuation: 2016-12-14
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: DOUBLE PUMP RF
• Version Model Number: 72204055
• Catalog Number: 72204055
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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)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	00885554037548 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K093409

FDA Product Code

• HRX: ARTHROSCOPE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-09-18

On-Brand Devices [DOUBLE PUMP RF]

• 00885554037609: FOOT PEDAL DOUBLE PUMP RF 2 PEDAL
• 00885554037593: FOOT PEDAL DOUBLE PUMP RF 4 PEDAL
• 00885554037555: CASSETTE DOUBLE PUMP SINGLE 100/BX
• 00885554037548: DOUBLE PUMP RF PATIENT CASSETTE 20/BX
• 00885554037524: CASSETTE DAY CASSETTE DBL PUMP RF
• 00885554037517: CABLE RF CABLE DBL PUMP RF