DynaSafety Instant Cold Pack, 4" x 5"

GUDID 00810180840545

For use whenever instant cold therapy is required

Dynarex Corporation

Hot/cold therapy pack, single-use

• Primary Device ID: 00810180840545
• NIH Device Record Key: 42ffd942-a378-4744-8721-f74a5bdc3438
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DynaSafety Instant Cold Pack, 4" x 5"
• Version Model Number: 4511UB-2
• Company DUNS: 008124539
• Company Name: Dynarex Corporation
• Device Count: 2
• 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: true
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810180840545 [Unit of Use]
GS1	00840117334779 [Package]; Contains: 00840117334786; Package: Case [36 Units]; In Commercial Distribution
GS1	00840117334786 [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: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2024-10-29
• Device Publish Date: 2024-03-08

On-Brand Devices [DynaSafety Instant Cold Pack, 4" x 5" ]

• 08401173347862: For use whenever instant cold therapy is required
• 00810180840545: For use whenever instant cold therapy is required