Merlin 605039

GUDID 30884527006483

Prep Applicator,PVP-I/IPA

Cardinal Health, Inc.

Surgical scrub preparation kit

• Primary Device ID: 30884527006483
• NIH Device Record Key: c0872b33-843e-4bd6-b1f6-67e7615cd001
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Merlin
• Version Model Number: 605039
• Catalog Number: 605039
• Company DUNS: 080935429
• Company Name: Cardinal Health, Inc.
• 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: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com

Device Dimensions

• Total Volume: 39 Milliliter
• Total Volume: 39 Milliliter

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT

Device Identifiers

Device Issuing Agency	Device ID
GS1	10884527006489 [Package]; Contains: 20884527006486; Package: PACK_OR_INNER_PACK [10 Units]; In Commercial Distribution
GS1	20884527006486 [Primary]
GS1	30884527006483 [Package]; Contains: 20884527006486; Package: CASE [20 Units]; In Commercial Distribution

FDA Product Code

• GEC: BRUSH, SCRUB, OPERATING-ROOM

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-02-15
• Device Publish Date: 2018-06-30

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