Meijer, instant cold pack

GUDID 00708820957473

Meijer-Instant Cold Pack

MEIJER, INC.

Hot/cold therapy pack, single-use

• Primary Device ID: 00708820957473
• NIH Device Record Key: fc0c0c9a-2503-4384-affd-3b81400c5ac7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Meijer, instant cold pack
• Version Model Number: 3650109
• Company DUNS: 006959555
• Company Name: MEIJER, 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: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00708820957473 [Primary]

FDA Product Code

• IMD: Pack, Hot Or Cold, Disposable

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: 2020-07-29
• Device Publish Date: 2020-07-21

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