HTT,78X30,OAK,PF Black,A09,A03

GUDID 00840314803597

Hausmann Enterprises, LLC

Examination/treatment table, manual

• Primary Device ID: 00840314803597
• NIH Device Record Key: b118a5f6-cca2-4f36-a790-8654c4903456
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HTT,78X30,OAK,PF Black,A09,A03
• Version Model Number: HTT-3078-L01V23-A09A03
• Company DUNS: 001892660
• Company Name: Hausmann Enterprises, LLC
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• 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	00840314803597 [Primary]

FDA Product Code

• INT: Plinth

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: 2022-08-24
• Device Publish Date: 2022-08-16

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