FlexBand

GUDID 00850003396019

FlexBand 0.5 x 32 Strip

Artelon

Polyester suture, bioabsorbable, monofilament

• Primary Device ID: 00850003396019
• NIH Device Record Key: 8ebba18e-a74d-4aa8-8809-28ad1bc1d208
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FlexBand
• Version Model Number: 31057
• Company DUNS: 066284070
• Company Name: Artelon
• 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: false
• Serial Number: true
• 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	00850003396019 [Primary]

FDA Product Code

• FTL: Mesh, Surgical, Polymeric

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: 2019-12-24
• Device Publish Date: 2019-12-16

On-Brand Devices [FlexBand]

• 00850003396118: FlexBand 0.5 x 24 Strip
• 00850003396019: FlexBand 0.5 x 32 Strip
• 00850003396002: FlexBand 0.3 x 32 Strip
• 00850003396132: FlexBand 0.7 x 24 Strip
• 00850003396125: FlexBand 0.3 x 24 Strip
• 00868047000397: FlexBand 0.7 x 32 Strip
• 00868047000380: FlexBand 0.7 x 16 Strip
• 00868047000373: FlexBand 0.7 x 8 Strip
• 00868047000366: FlexBand 0.5 x 16 Strip
• 00868047000359: FlexBand 0.5 x 8 Strip
• 00868047000342: FlexBand 0.3 x 16 Strip
• 00868047000335: FlexBand 0.3 x 8 Strip
• 00868047000328: FlexBand 6 x 9 Mesh
• 00868047000311: FlexBand 3 x 4 Mesh
• 00868047000304: FlexBand 4 x 6 Mesh