TiMESH

GUDID 04042301097668

Ti-Mesh 12" X 12" Light 35g/m²

pfm medical titanium gmbh

Abdominal hernia surgical mesh, synthetic polymer, non-bioabsorbable

• Primary Device ID: 04042301097668
• NIH Device Record Key: 35ca4234-b84a-49bd-a306-d206986d89a4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TiMESH
• Version Model Number: 6000139
• Company DUNS: 344675942
• Company Name: pfm medical titanium gmbh
• 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: 7607588749
• Email: regulatory@pfmmedicalusa.com
• Phone: 7607588749
• Email: regulatory@pfmmedicalusa.com
• Phone: 7607588749
• Email: regulatory@pfmmedicalusa.com
• Phone: 7607588749
• Email: regulatory@pfmmedicalusa.com
• Phone: 7607588749
• Email: regulatory@pfmmedicalusa.com
• Phone: 7607588749
• Email: regulatory@pfmmedicalusa.com
• Phone: 7607588749
• Email: regulatory@pfmmedicalusa.com
• Phone: 7607588749
• Email: regulatory@pfmmedicalusa.com
• Phone: 7607588749
• Email: regulatory@pfmmedicalusa.com
• Phone: 7607588749
• Email: regulatory@pfmmedicalusa.com
• Phone: 7607588749
• Email: regulatory@pfmmedicalusa.com
• Phone: 7607588749
• Email: regulatory@pfmmedicalusa.com
• Phone: 7607588749
• Email: regulatory@pfmmedicalusa.com
• Phone: 7607588749
• Email: regulatory@pfmmedicalusa.com
• Phone: 7607588749
• Email: regulatory@pfmmedicalusa.com
• Phone: 7607588749
• Email: regulatory@pfmmedicalusa.com
• Phone: 7607588749
• Email: regulatory@pfmmedicalusa.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04042301097668 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K031225

FDA Product Code

• OXJ: Mesh, Surgical, Non-Absorbable, Large Abdominal Wall Defects

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-12-17
• Device Publish Date: 2019-12-09

On-Brand Devices [TiMESH]

• 04042301144348: Ti-Mesh 1.4" X 4" Strong 65g/m²
• 04042301144324: Ti-Mesh 1.4" X 4" Light 35g/m²
• 04042301097668: Ti-Mesh 12" X 12" Light 35g/m²
• 04042301097651: Ti-Mesh 6" X 8" Light 35g/m²
• 04042301097576: Ti-Mesh 4" X 6" Light 35 g/m²
• 04042301097552: Ti-Mesh 4" X 6" Extra Light 16 g/m²
• 04042301097606: Ti-Mesh 6" X 6" Light 35g/m²