| Primary Device ID | 00304040018682 |
| NIH Device Record Key | 08ddc236-6ca8-420a-a5ed-8df5dc798c4e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Henry Schein Tray Barriers |
| Version Model Number | 1014275 |
| Catalog Number | 1014275 |
| Company DUNS | 012430880 |
| Company Name | HENRY SCHEIN, INC. |
| Device Count | 500 |
| DM Exempt | true |
| Pre-market Exempt | false |
| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 00304040018682 [Primary] |
| GS1 | 20304040018686 [Unit of Use] |
| MMP | Cover, barrier, protective |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-24 |
| 00304040188200 - Henry Schein | 2024-11-20 Zirlux Nightguard & Splint Print Resin - Flexible |
| 00304040188217 - Henry Schein | 2024-11-20 Zirlux Nightguard & Splint Print Resin - Rigid |
| 00304040188248 - Henry Schein | 2024-11-20 Zirlux Surgical Guides Print Resin |
| 00304040188262 - Henry Schein | 2024-11-20 Pack Citrus Cath F/ Citrus Cardiology |
| 00304040188279 - Henry Schein | 2024-11-20 Pack Vein Ablation F/ AZ Vein and Laser Institute |
| 10304040081300 - Henry Schein | 2024-11-07 Maxima Suture PGA Undyed NP-3 |
| 10304040081317 - Henry Schein | 2024-11-07 Maxima Suture PGA Undyed NP-3 |
| 10304040081324 - Henry Schein | 2024-11-07 Maxima Suture PGA Undyed NPS-2 |