Artisential Maryland Dissector

GUDID 08800042701055

Sterile Single-use Manual Surgical Instrument for general use

LIVSMED

Rigid endoscopic tissue manipulation forceps, single-use

• Primary Device ID: 08800042701055
• NIH Device Record Key: 65fab30b-c607-41b4-9b3a-f47884353e6f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Artisential Maryland Dissector
• Version Model Number: AUD01-LV
• Company DUNS: 688360116
• Company Name: LIVSMED
• Device Count: 1
• DM Exempt: false
• 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: 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: 833-548-7633
• Email: infousa@livsmed.com
• Phone: 833-548-7633
• Email: infousa@livsmed.com
• Phone: 833-548-7633
• Email: infousa@livsmed.com
• Phone: 833-548-7633
• Email: infousa@livsmed.com
• Phone: 833-548-7633
• Email: infousa@livsmed.com
• Phone: 833-548-7633
• Email: infousa@livsmed.com
• Phone: 833-548-7633
• Email: infousa@livsmed.com
• Phone: 833-548-7633
• Email: infousa@livsmed.com
• Phone: 833-548-7633
• Email: infousa@livsmed.com
• Phone: 833-548-7633
• Email: infousa@livsmed.com
• Phone: 833-548-7633
• Email: infousa@livsmed.com
• Phone: 833-548-7633
• Email: infousa@livsmed.com
• Phone: 833-548-7633
• Email: infousa@livsmed.com
• Phone: 833-548-7633
• Email: infousa@livsmed.com
• Phone: 833-548-7633
• Email: infousa@livsmed.com
• Phone: 833-548-7633
• Email: infousa@livsmed.com
• Phone: 833-548-7633
• Email: infousa@livsmed.com
• Phone: 833-548-7633
• Email: infousa@livsmed.com

Device Dimensions

• Shaft Length: 38 Centimeter
• Shaft Length: 38 Centimeter
• Shaft Length: 38 Centimeter
• Shaft Length: 38 Centimeter
• Shaft Length: 38 Centimeter
• Shaft Length: 38 Centimeter
• Shaft Length: 38 Centimeter
• Shaft Length: 38 Centimeter
• Shaft Length: 38 Centimeter
• Shaft Length: 38 Centimeter
• Shaft Length: 38 Centimeter
• Shaft Length: 38 Centimeter
• Shaft Length: 38 Centimeter
• Shaft Length: 38 Centimeter
• Shaft Length: 38 Centimeter
• Shaft Length: 38 Centimeter
• Shaft Length: 38 Centimeter
• Shaft Length: 38 Centimeter

Operating and Storage Conditions

• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800042701055 [Primary]

FDA Product Code

• MDM: Instrument, Manual, Surgical, General Use

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: 2024-01-30
• Device Publish Date: 2024-01-22

On-Brand Devices [Artisential Maryland Dissector]

• 08800042701079: Sterile Single-use Manual Surgical Instrument for general use
• 08800042701055: Sterile Single-use Manual Surgical Instrument for general use
• 08800042700294: Sterile Single-use Manual Surgical Instrument for general use
• 08800042700133: Sterile Single-use Manual Surgical Instrument for general use