Primary Device ID | 00883205032157 |
NIH Device Record Key | 512ef27b-677c-4c68-bee3-46e7417007e0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Slide Packer |
Version Model Number | 833 |
Catalog Number | 833 |
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 |
Phone | +1(801)572-4200 |
customerservice@ultradent.com | |
Phone | +1(801)572-4200 |
customerservice@ultradent.com | |
Phone | +1(801)572-4200 |
customerservice@ultradent.com | |
Phone | +1(801)572-4200 |
customerservice@ultradent.com | |
Phone | +1(801)572-4200 |
customerservice@ultradent.com | |
Phone | +1(801)572-4200 |
customerservice@ultradent.com | |
Phone | +1(801)572-4200 |
customerservice@ultradent.com | |
Phone | +1(801)572-4200 |
customerservice@ultradent.com | |
Phone | +1(801)572-4200 |
customerservice@ultradent.com | |
Phone | +1(801)572-4200 |
customerservice@ultradent.com | |
Phone | +1(801)572-4200 |
customerservice@ultradent.com | |
Phone | +1(801)572-4200 |
customerservice@ultradent.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00883205032157 [Primary] |
EJB | HANDLE, INSTRUMENT, DENTAL |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-08-27 |
Device Publish Date | 2025-08-19 |
00883205004833 | Slide Packer, Regular |
00883205004789 | Slide Packer, Small |
00883205032157 | Slide Packer, Regular |
00883205032164 | Slide Packer, Small |