Drape 610-1241, 610-1241-5

GUDID 00841436102766

Sterile (32.4 x 27.9cm) polyethylene drape

CIVCO MEDICAL INSTRUMENTS CO., INC.

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• Primary Device ID: 00841436102766
• NIH Device Record Key: a5661c37-6468-45c1-ba22-7d8c6bd0aac5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Drape
• Version Model Number: 610-1241, 610-1241-5
• Catalog Number: 610-1241, 610-1241-5
• Company DUNS: 134614411
• Company Name: CIVCO MEDICAL INSTRUMENTS CO., INC.
• 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: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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: +1(319)248-6502
• Email: regulatory@civco.com
• Phone: +1(319)248-6502
• Email: regulatory@civco.com
• Phone: +1(319)248-6502
• Email: regulatory@civco.com
• Phone: +1(319)248-6502
• Email: regulatory@civco.com
• Phone: +1(319)248-6502
• Email: regulatory@civco.com
• Phone: +1(319)248-6502
• Email: regulatory@civco.com
• Phone: +1(319)248-6502
• Email: regulatory@civco.com
• Phone: +1(319)248-6502
• Email: regulatory@civco.com
• Phone: +1(319)248-6502
• Email: regulatory@civco.com
• Phone: +1(319)248-6502
• Email: regulatory@civco.com

Device Dimensions

• Width: 27.9 Centimeter
• Length: 32.4 Centimeter
• Width: 27.9 Centimeter
• Length: 32.4 Centimeter
• Width: 27.9 Centimeter
• Length: 32.4 Centimeter
• Width: 27.9 Centimeter
• Length: 32.4 Centimeter
• Width: 27.9 Centimeter
• Length: 32.4 Centimeter
• Width: 27.9 Centimeter
• Length: 32.4 Centimeter
• Width: 27.9 Centimeter
• Length: 32.4 Centimeter
• Width: 27.9 Centimeter
• Length: 32.4 Centimeter
• Width: 27.9 Centimeter
• Length: 32.4 Centimeter
• Width: 27.9 Centimeter
• Length: 32.4 Centimeter

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Keep Away from Sunlight
• Storage Environment Temperature: Between 52 Degrees Fahrenheit and 85 Degrees Fahrenheit
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away from Sunlight
• Storage Environment Temperature: Between 52 Degrees Fahrenheit and 85 Degrees Fahrenheit
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away from Sunlight
• Storage Environment Temperature: Between 52 Degrees Fahrenheit and 85 Degrees Fahrenheit
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away from Sunlight
• Storage Environment Temperature: Between 52 Degrees Fahrenheit and 85 Degrees Fahrenheit
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away from Sunlight
• Storage Environment Temperature: Between 52 Degrees Fahrenheit and 85 Degrees Fahrenheit
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away from Sunlight
• Storage Environment Temperature: Between 52 Degrees Fahrenheit and 85 Degrees Fahrenheit
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away from Sunlight
• Storage Environment Temperature: Between 52 Degrees Fahrenheit and 85 Degrees Fahrenheit
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away from Sunlight
• Storage Environment Temperature: Between 52 Degrees Fahrenheit and 85 Degrees Fahrenheit
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away from Sunlight
• Storage Environment Temperature: Between 52 Degrees Fahrenheit and 85 Degrees Fahrenheit
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away from Sunlight
• Storage Environment Temperature: Between 52 Degrees Fahrenheit and 85 Degrees Fahrenheit

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841436102759 [Package]; Contains: 10841436102763; Package: [5 Units]; In Commercial Distribution
GS1	00841436102766 [Package]; Contains: 10841436102763; Package: [24 Units]; In Commercial Distribution
GS1	10841436102763 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K970513

FDA Product Code

• ITX: Transducer, ultrasonic, diagnostic

Sterilization

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

[00841436102766]

Ethylene Oxide

[00841436102766]

Ethylene Oxide

[00841436102766]

Ethylene Oxide

[00841436102766]

Ethylene Oxide

[00841436102766]

Ethylene Oxide

[00841436102766]

Ethylene Oxide

[00841436102766]

Ethylene Oxide

[00841436102766]

Ethylene Oxide

[00841436102766]

Ethylene Oxide

[00841436102766]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2021-09-06
• Device Publish Date: 2017-08-22

On-Brand Devices [Drape]

• 00841436120883: Non-sterile (32.4x27.9cm) polyethlene drape
• 00841436120876: Non-sterile (50.8x71.1cm) polyethlene drape
• 00841436102766: Sterile (32.4 x 27.9cm) polyethylene drape
• 00841436101820: Sterile (15.2 x 25.4cm) polyethylene cover
• 00841436101790: Sterile polyethylene drape (50.8 x 71.1cm)