POSTERIOR MOLAR PAD 700-007T

GUDID D909700007T1

POSTERIOR MOLAR PAD TIP

Ortho Arch Company Inc

Dental mould

• Primary Device ID: D909700007T1
• NIH Device Record Key: a736d86c-eed2-47b2-b90b-7244a1c6d8e8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: POSTERIOR MOLAR PAD
• Version Model Number: 700-007T
• Catalog Number: 700-007T
• Company DUNS: 020956330
• Company Name: Ortho Arch Company Inc
• 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: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D909700007T1 [Primary]

FDA Product Code

• EGD: Wax, Dental, Intraoral

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: 2023-07-05
• Device Publish Date: 2023-06-27

On-Brand Devices [POSTERIOR MOLAR PAD]

• D909700007T1: POSTERIOR MOLAR PAD TIP
• D90970000711: POSTERIOR MOLAR PAD TIPS & HANDLE (10 TIPS)