KerraPro KPRO30

GUDID 05060077234086

CRAWFORD HEALTHCARE LIMITED

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• Primary Device ID: 05060077234086
• NIH Device Record Key: bd827ab8-3796-40ff-a91c-c5726fc34737
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KerraPro
• Version Model Number: Heel
• Catalog Number: KPRO30
• Company DUNS: 543740310
• Company Name: CRAWFORD HEALTHCARE LIMITED
• 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: false
• 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: false

Customer Support Contacts

• Phone: +4401565654920
• Email: andrew.jackson@acelity.com
• Phone: +4401565654920
• Email: andrew.jackson@acelity.com
• Phone: +4401565654920
• Email: andrew.jackson@acelity.com
• Phone: +4401565654920
• Email: andrew.jackson@acelity.com
• Phone: +4401565654920
• Email: andrew.jackson@acelity.com
• Phone: +4401565654920
• Email: andrew.jackson@acelity.com
• Phone: +4401565654920
• Email: andrew.jackson@acelity.com
• Phone: +4401565654920
• Email: andrew.jackson@acelity.com
• Phone: +4401565654920
• Email: andrew.jackson@acelity.com
• Phone: +4401565654920
• Email: andrew.jackson@acelity.com
• Phone: +4401565654920
• Email: andrew.jackson@acelity.com
• Phone: +4401565654920
• Email: andrew.jackson@acelity.com
• Phone: +4401565654920
• Email: andrew.jackson@acelity.com
• Phone: +4401565654920
• Email: andrew.jackson@acelity.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	05060077230408 [Package]; Contains: 05060077230422; Package: Carton [2 Units]; In Commercial Distribution
GS1	05060077230422 [Primary]
GS1	05060077234086 [Package]; Contains: 05060077230408; Package: Shipper [32 Units]; In Commercial Distribution

FDA Product Code

• FMP: Protector, Skin Pressure

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-10-09
• Device Publish Date: 2019-10-01

On-Brand Devices [KerraPro]

• 05060077234123: 20 x 1 x 0.1in
• 05060077234116: 12 x 2 x 0.1in
• 05060077230392: 4 x 4 x 0.5in
• 05060077234093: 4 x 4 x 0.1 in
• 05060077234086: Heel