FIRSTPASSST 22-4039

GUDID 00817470012316

DFP SUTURE PASSER STANDARD

Smith & Nephew, Inc.

Suturing unit, reusable

• Primary Device ID: 00817470012316
• NIH Device Record Key: 196e2a07-17a5-4de8-8d58-70a0c083f293
• Commercial Distribution Discontinuation: 2018-09-01
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: FIRSTPASSST
• Version Model Number: 22-4039
• Catalog Number: 22-4039
• Company DUNS: 109903521
• Company Name: Smith & Nephew, Inc.
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817470012316 [Primary]

FDA Product Code

• HWQ: PASSER

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2020-02-06
• Device Publish Date: 2017-11-13

On-Brand Devices [FIRSTPASSST]

• 00817470012316: DFP SUTURE PASSER STANDARD
• 00817470012309: DISP FIRSTPASS STR PASSR SELF