Fischer Ultrapak Packer 172

GUDID 00883205019752

Fischer's Ultrapak Packer 90° Regular

ULTRADENT PRODUCTS, INC.

Dental curette, basic

• Primary Device ID: 00883205019752
• NIH Device Record Key: 39705b80-a41d-42a2-a893-96325c05011f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Fischer Ultrapak Packer
• Version Model Number: 172
• Catalog Number: 172
• Company DUNS: 013369913
• Company Name: ULTRADENT PRODUCTS, 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: 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(801)572-4200
• Email: customerservice@ultradent.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00883205019752 [Primary]

FDA Product Code

• EJB: HANDLE, INSTRUMENT, DENTAL

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00883205019752]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-05-29
• Device Publish Date: 2018-04-28

On-Brand Devices [Fischer Ultrapak Packer]

• 00883205019769: Fischer's Ultrapak Packer 90° Small
• 00883205019752: Fischer's Ultrapak Packer 90° Regular
• 00883205019288: Fischer's Ultrapak Packer 45° Regular
• 00883205015433: Fischer's Ultrapak Packer 45° Small