No-Scalpel Vasectomy LV-FCP-858

GUDID 15055515600285

No-Scalpel Vasectomy Forcep

FEMCARE LIMITED

Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable

• Primary Device ID: 15055515600285
• NIH Device Record Key: 85d9cb47-e4bf-4e37-a3bd-94607f99a2e7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: No-Scalpel Vasectomy
• Version Model Number: Forceps
• Catalog Number: LV-FCP-858
• Company DUNS: 500218573
• Company Name: FEMCARE LIMITED
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	15055515600285 [Primary]

FDA Product Code

• KOA: Surgical Instruments, G-U, Manual (And Accessories)

Sterilization

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

[15055515600285]

Moist Heat or Steam Sterilization

[15055515600285]

Moist Heat or Steam Sterilization

[15055515600285]

Moist Heat or Steam Sterilization

[15055515600285]

Moist Heat or Steam Sterilization

[15055515600285]

Moist Heat or Steam Sterilization

[15055515600285]

Moist Heat or Steam Sterilization

[15055515600285]

Moist Heat or Steam Sterilization

[15055515600285]

Moist Heat or Steam Sterilization

[15055515600285]

Moist Heat or Steam Sterilization

[15055515600285]

Moist Heat or Steam Sterilization

[15055515600285]

Moist Heat or Steam Sterilization

[15055515600285]

Moist Heat or Steam Sterilization

[15055515600285]

Moist Heat or Steam Sterilization

[15055515600285]

Moist Heat or Steam Sterilization

[15055515600285]

Moist Heat or Steam Sterilization

[15055515600285]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-06-15
• Device Publish Date: 2023-06-07

On-Brand Devices [No-Scalpel Vasectomy]

• 15055515600308: No-Scalpel Vasectomy Ring Clamp, 4.0mm
• 15055515600292: No-Scalpel Vasectomy 4.0mm kit
• 15055515600285: No-Scalpel Vasectomy Forcep
• 15055515600278: No-Scalpel Vasectomy 3.5mm kit
• 15055515600261: No-Scalpel Vasectomy Ring Clamp, 3.5mm