ProCare Dent 30 P

GUDID 04029577143510

Chemische Fabrik Dr. Weigert GmbH & Co. KG

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• Primary Device ID: 04029577143510
• NIH Device Record Key: 7b404100-3247-4602-b2e6-388212f0e716
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ProCare Dent 30 P
• Version Model Number: 4029577143510
• Company DUNS: 316788397
• Company Name: Chemische Fabrik Dr. Weigert GmbH & Co. KG
• 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: 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	04029577143510 [Primary]

FDA Product Code

• FLG: Cleaner, Ultrasonic, Medical Instrument

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: 2022-07-11
• Device Publish Date: 2022-07-02

On-Brand Devices [ProCare Dent 30 P]

• 04029577143497: 4029577143497
• 04029577155094: 4029577155094
• 04029577155087: 4029577155087
• 04029577143510: 4029577143510
• 04029577143503: 4029577143503