ColdSPOT

GUDID 20815137021088

Cold Therapy Packs, 2.0x3.0" gel pack, with Florals

Beekley Corporation

Hot/cold therapy pack, single-use

• Primary Device ID: 20815137021088
• NIH Device Record Key: 70a5ec5f-3991-49ec-b4d2-c303a93d1f76
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ColdSPOT
• Version Model Number: 502
• Company DUNS: 001157841
• Company Name: Beekley Corporation
• Device Count: 34
• 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: 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	00815137021084 [Primary]
GS1	10815137021081 [Unit of Use]
GS1	20815137021088 [Package]; Contains: 00815137021084; Package: [2 Units]; In Commercial Distribution

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: 2019-07-30
• Device Publish Date: 2019-07-22

On-Brand Devices [ColdSPOT]

• 00815137021992: Cold Therapy Packs, 2.0x3.0" gel pack
• 00815137021985: Cold Therapy Packs, 2.0x3.0" gel pack, with Florals
• 00815137021978: Cold Therapy Packs, 2.75x3.0" gel pack
• 20815137021088: Cold Therapy Packs, 2.0x3.0" gel pack, with Florals
• 20815137021071: Cold Therapy Packs, 2.75x3.0" gel pack
• 00815137021060: Cold Therapy Packs, 2.0x3.0" gel pack