Kennestone T & A

GUDID 00817395021981

Kennestone T & A

PACKROOM LLC

Birthing/delivery kit Birthing/delivery kit Birthing/delivery kit Birthing/delivery kit Birthing/delivery kit Birthing/delivery kit Birthing/delivery kit Birthing/delivery kit Birthing/delivery kit Birthing/delivery kit Birthing/delivery kit Birthing/delivery kit

• Primary Device ID: 00817395021981
• NIH Device Record Key: c241108c-057e-4167-a3cb-629fda8cbc4a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Kennestone T & A
• Version Model Number: WK380
• Company DUNS: 015179820
• Company Name: PACKROOM LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• 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	00817395021981 [Primary]

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-10-29
• Device Publish Date: 2020-10-21

On-Brand Devices [Kennestone T & A]

• 00817395021981: Kennestone T & A
• 00817395022933: Kennestone T & A (156177)