SpiraLith Ca

GUDID 00860008449849

Micropore, Inc.

Carbon dioxide absorber, single-use

• Primary Device ID: 00860008449849
• NIH Device Record Key: 95f3c694-6b73-4c6d-8c52-d22338b38920
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SpiraLith Ca
• Version Model Number: Rx-3903C
• Company DUNS: 042903703
• Company Name: Micropore, 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: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: true
• 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	00860008449849 [Primary]
GS1	10860008449846 [Package]; Package: Box [6 Units]; In Commercial Distribution

FDA Product Code

• CBL: Absorbent, Carbon-Dioxide

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: 2022-10-03
• Device Publish Date: 2022-09-23

On-Brand Devices [SpiraLith Ca]

• 00860008449849: Rx-3903C
• 10860008449839: Rx-3719C
• 00860008449801: Rx-2903C