Bowie Dick Type Test CI-BDTLF

GUDID M985CIBDTLF0

ProChem B-D Bowie Dick Type Test pack

MESA LABORATORIES, INC.

Chemical/physical sterilization process indicator

• Primary Device ID: M985CIBDTLF0
• NIH Device Record Key: 3d4a169c-3a1f-4ee8-8191-74991a348b92
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bowie Dick Type Test
• Version Model Number: ProChem
• Catalog Number: CI-BDTLF
• Company DUNS: 102530326
• Company Name: MESA LABORATORIES, 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: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M985CIBDTLF0 [Primary]
HIBCC	M985CIBDTLF1 [Package]; Package: Pack [20 Units]; In Commercial Distribution
HIBCC	M985CIBDTLF2 [Package]; Package: Case [80 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: 5
• Public Version Date: 2021-02-19
• Device Publish Date: 2016-10-24

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