Silicone MCP SMCP-500-05-WW

GUDID 00885556856871

SILICONE MCP SZ 05

Smith & Nephew, Inc.

Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece

• Primary Device ID: 00885556856871
• NIH Device Record Key: 6483bfbe-6807-4ad7-ab45-53c18100ccca
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Silicone MCP
• Version Model Number: SMCP-500-05-WW
• Catalog Number: SMCP-500-05-WW
• Company DUNS: 045483575
• 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
• 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	00885556856871 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K022892

FDA Product Code

• KYJ: Prosthesis, finger, constrained, polymer

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2023-09-07
• Device Publish Date: 2022-12-22

On-Brand Devices [Silicone MCP]

• 00885556857137: SMCP TRIAL SZ 50
• 00885556857120: SMCP TRIAL SZ 40
• 00885556857113: SMCP TRIAL SZ 30
• 00885556857106: SMCP TRIAL SZ 20
• 00885556857090: SMCP TRIAL SZ 10
• 00885556857083: SMCP TRIAL SZ. 05
• 00885556856925: SILICONE MCP SZ 50
• 00885556856918: SILICONE MCP SZ 40
• 00885556856901: SILICONE MCP SZ 30
• 00885556856895: SILICONE MCP SZ 20
• 00885556856888: SILICONE MCP SZ 10
• 00885556856871: SILICONE MCP SZ 05