GIBSON

GUDID 00366975002235

suture 4-0 PTFE 18" FS-3 BX12

BENCO DENTAL SUPPLY CO.

Polytetrafluoroethylene suture

• Primary Device ID: 00366975002235
• NIH Device Record Key: 10f27a30-b53a-48c7-aa65-fe5710f24679
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GIBSON
• Version Model Number: 5067-661
• Company DUNS: 015108087
• Company Name: BENCO DENTAL SUPPLY CO.
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00366975002235 [Primary]
GS1	10366975002232 [Package]; Package: [12 Units]; In Commercial Distribution

FDA Product Code

• NBY: Suture, Surgical, Nonabsorbable, Expanded, Polytetraflouroethylene

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: 2018-06-27
• Device Publish Date: 2016-09-23

On-Brand Devices [GIBSON]

• 10366975002287: suture 6-0 PTFE 18" P-3 BX12
• 10366975002270: suture 5-0 PTFE 18" P-3 BX12
• 10366975002263: suture 4-0 PTFE 18" P-3 BX12
• 10366975002256: suture 4-0 PTFE 18" PS-2 BX12
• 10366975002249: suture 4-0 PTFE 18" TF BX12
• 00366975002235: suture 4-0 PTFE 18" FS-3 BX12
• 00366975002228: suture 3-0 PTFE 18" FS-3 BX12
• 00366975002211: suture 3-0 PTFE 18" FS-2 BX12
• 00366975002204: suture 2-0 PTFE 18" FS-2 BX12
• 00366975016621: 4845-901
• 00366975016614: 4845-894
• 00366975016607: 4845-885
• 00366975016591: 4845-867
• 00366975016584: 4845-858
• 00366975016577: 4845-830