Spark

GUDID 00681131145855

Waterfilled Fish Teethers

WAL-MART STORES, INC.

Teething device, fluid-filled Teething device, fluid-filled

• Primary Device ID: 00681131145855
• NIH Device Record Key: 953facf4-17b8-4f5d-b6b0-4efcd13df5ba
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Spark
• Version Model Number: 26201
• Company DUNS: 051957769
• Company Name: WAL-MART STORES, INC.
• Device Count: 2
• 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: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00681131145855 [Primary]
GS1	01681131145855 [Unit of Use]

FDA Product Code

• KKO: Ring, Teething, Fluid-Filled

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-08-31

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