SteriTec EO Sterilization Indicator Tape CI 124/1

GUDID 10814434020162

STERITEC PRODUCT MFG. CO., INC.

Sterilization packaging tape

• Primary Device ID: 10814434020162
• NIH Device Record Key: 6ca74d3e-8403-44df-9d1e-37635b5b07c7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SteriTec EO Sterilization Indicator Tape
• Version Model Number: CI 124/1
• Catalog Number: CI 124/1
• Company DUNS: 622223196
• Company Name: STERITEC PRODUCT MFG. CO., INC.
• 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: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Operating and Storage Conditions

• Storage Environment Temperature: Between 10 Degrees Celsius and 38 Degrees Celsius
• Storage Environment Temperature: Between 10 Degrees Celsius and 38 Degrees Celsius
• Storage Environment Temperature: Between 10 Degrees Celsius and 38 Degrees Celsius
• Storage Environment Temperature: Between 10 Degrees Celsius and 38 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	00814434020165 [Primary]
GS1	10814434020162 [Package]; Contains: 00814434020165; Package: Case [36 Units]; In Commercial Distribution

FDA Product Code

• JOJ: Indicator, Physical/Chemical Sterilization Process

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-23

On-Brand Devices [SteriTec EO Sterilization Indicator Tape]

• 10814434020162: CI 124/1
• 10814434020155: CI 124/.75