ASSUFIL MONOFILAMENTO

GUDID 78033439360842

ASSUT EUROPE SPA

Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial

• Primary Device ID: 78033439360842
• NIH Device Record Key: 3b6634f3-58dc-4f71-9b0c-3708691c7fc6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ASSUFIL MONOFILAMENTO
• Version Model Number: 5FS65MHYSO
• Company DUNS: 654747567
• Company Name: ASSUT EUROPE SPA
• 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: true
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	78033439360842 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K150553

FDA Product Code

• NEW: Suture, Surgical, Absorbable, Polydioxanone

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: 2024-04-08
• Device Publish Date: 2024-03-29

On-Brand Devices [ASSUFIL MONOFILAMENTO]

• 78033439180655: 5FV57MHBS3YSL
• 78033439180648: 5FV57MHBS3YSL
• 78033439180631: 5FV60MHBS5YSO
• 78033439180563: 5FV60MH4YSO
• 78033439180556: 5FV60MHBD4YSO
• 78033439180549: 5FV60MHBD2YSL
• 78033439180532: 5FV60MH2YSL
• 78033439180525: 5FV60MHB1YSL
• 78033439180501: 5FV60MHB2YSO
• 78033439173565: FU61MHYSO
• 78033439173558: FU62MHYAB
• 78033439171400: 5FY59MMYSG
• 78033439171394: 5FY58MMYSL
• 78033439171387: 5FY58MMYSI
• 58033439168352: 06F.L12
• 58033439090912: 06F.L.-232
• 78033439181331: 5FV60MHB16YSV
• 08033439168456: 5FV57MHYAB
• 08033439168449: 5FV60MHYSO
• 08033439168432: 5FV60MHYSL
• 08033439005263: FS573M
• 08033439005225: FU534M
• 08033439005195: FV516M
• 08033439005096: FW515M
• 58033439195860: 06F.L.12DN/2/0W/6
• 58033439195853: 06F.L.23DN/2/0W/18
• 58033439195785: 06F.L.23DN/2/0/18
• 58033439195778: 06F.L.23DN/0/18
• 58033439195761: 06F.L.12DN/2/0/6
• 58033439195754: 06F.L.12DN/6
• 08033439195872: 04F.L.232DN/DS/W/20
• 08033439195834: 04F.L.232DN/DS/20
• 78033439195956: 10F.L./R/C/18/W/4
• 78033439195949: 10F.L.R/C/18/4
• 78033439196519: 10F.L./R/C/15/W/4
• 58033439196508: 06F.L.23DN/2/0W/15
• 58033439196492: 06F.L.12DN/2/0W/10
• 78033439196977: 10F.L./R/C/15/4
• 58033439196966: 06F.L.23DN/15
• 58033439196959: 06F.L.12DN/10
• 58033439196751: 06F.L.12DN/7/S/C
• 58033439197031: 06F.L.23DN/10
• 78033439360880: 5FW69MMYSL
• 78033439360873: 5FW69MMYSI
• 78033439360866: 5FW66MMYSG
• 78033439360859: 5FS61MHYAB
• 78033439360842: 5FS65MHYSO
• 78033439360835: 5FS65MHYSL