Seracult Tape Fecal Occult Blood Test

GUDID 30818087013117

Seracult Tape Fecal Occult Blood Test

PROPPER MANUFACTURING COMPANY, INC.

Faecal occult blood IVD, reagent

• Primary Device ID: 30818087013117
• NIH Device Record Key: e275c9c6-2e88-4afe-bba7-e8009e73a302
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Seracult Tape Fecal Occult Blood Test
• Version Model Number: 37901000
• Company DUNS: 001483130
• Company Name: PROPPER MANUFACTURING COMPANY, INC.
• Device Count: 2
• 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
GS1	10818087013113 [Unit of Use]
GS1	30818087013117 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K834297

FDA Product Code

• KHE: Reagent, Occult Blood

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: 2019-03-22
• Device Publish Date: 2019-03-14

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