Maxicide 1022866
GUDID 00304040003947
Sterilizing and Disinfecting Solution
HENRY SCHEIN, INC.
Glutaraldehyde device sterilant Glutaraldehyde device sterilant Glutaraldehyde device sterilant Glutaraldehyde device sterilant Glutaraldehyde device sterilant Glutaraldehyde device sterilant Glutaraldehyde device sterilant Glutaraldehyde device sterilant Glutaraldehyde device sterilant Glutaraldehyde device sterilant Glutaraldehyde device sterilant Glutaraldehyde device sterilant Glutaraldehyde device sterilant Glutaraldehyde device sterilant Glutaraldehyde device sterilant Glutaraldehyde device sterilant Glutaraldehyde device sterilant Glutaraldehyde device sterilant Glutaraldehyde device sterilant| Primary Device ID | 00304040003947 |
| NIH Device Record Key | 23b4da14-86eb-4fda-999d-043a6b3d4a7b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Maxicide |
| Version Model Number | 1022866 |
| Catalog Number | 1022866 |
| Company DUNS | 012430880 |
| Company Name | HENRY SCHEIN, INC. |
| Device Count | 1 |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
Device Dimensions
| Total Volume | 3.785 Liter |
| Total Volume | 3.785 Liter |
| Total Volume | 3.785 Liter |
| Total Volume | 3.785 Liter |
| Total Volume | 3.785 Liter |
| Total Volume | 3.785 Liter |
| Total Volume | 3.785 Liter |
| Total Volume | 3.785 Liter |
| Total Volume | 3.785 Liter |
| Total Volume | 3.785 Liter |
| Total Volume | 3.785 Liter |
| Total Volume | 3.785 Liter |
| Total Volume | 3.785 Liter |
| Total Volume | 3.785 Liter |
| Total Volume | 3.785 Liter |
| Total Volume | 3.785 Liter |
| Total Volume | 3.785 Liter |
| Total Volume | 3.785 Liter |
| Total Volume | 3.785 Liter |
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *STORE AT ROOM TEMPERATURE |
| Special Storage Condition, Specify | Between 0 and 0 *STORE AT ROOM TEMPERATURE |
| Special Storage Condition, Specify | Between 0 and 0 *STORE AT ROOM TEMPERATURE |
| Special Storage Condition, Specify | Between 0 and 0 *STORE AT ROOM TEMPERATURE |
| Special Storage Condition, Specify | Between 0 and 0 *STORE AT ROOM TEMPERATURE |
| Special Storage Condition, Specify | Between 0 and 0 *STORE AT ROOM TEMPERATURE |
| Special Storage Condition, Specify | Between 0 and 0 *STORE AT ROOM TEMPERATURE |
| Special Storage Condition, Specify | Between 0 and 0 *STORE AT ROOM TEMPERATURE |
| Special Storage Condition, Specify | Between 0 and 0 *STORE AT ROOM TEMPERATURE |
| Special Storage Condition, Specify | Between 0 and 0 *STORE AT ROOM TEMPERATURE |
| Special Storage Condition, Specify | Between 0 and 0 *STORE AT ROOM TEMPERATURE |
| Special Storage Condition, Specify | Between 0 and 0 *STORE AT ROOM TEMPERATURE |
| Special Storage Condition, Specify | Between 0 and 0 *STORE AT ROOM TEMPERATURE |
| Special Storage Condition, Specify | Between 0 and 0 *STORE AT ROOM TEMPERATURE |
| Special Storage Condition, Specify | Between 0 and 0 *STORE AT ROOM TEMPERATURE |
| Special Storage Condition, Specify | Between 0 and 0 *STORE AT ROOM TEMPERATURE |
| Special Storage Condition, Specify | Between 0 and 0 *STORE AT ROOM TEMPERATURE |
| Special Storage Condition, Specify | Between 0 and 0 *STORE AT ROOM TEMPERATURE |
| Special Storage Condition, Specify | Between 0 and 0 *STORE AT ROOM TEMPERATURE |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00304040003947 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K930284
FDA Product Code
| MED | Sterilant, medical devices |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-24 |
Devices Manufactured by HENRY SCHEIN, INC.
| 00304040177983 - Henry Schein | 2024-04-24 Maxi-Gard Dual Fabric Cover GowFalse, Blue |
| 00304040180440 - Henry Schein | 2024-04-24 Pack Breast F/ Lemmon Avenue Surgery Center |
| 00304040180457 - Henry Schein | 2024-04-24 Pack Vein F/ Richmond Vein Center |
| 00304040180464 - Henry Schein | 2024-04-24 Pack Vein F/ Cardiovascular Specialists of South Florida |
| 00304040185063 - Henry Schein | 2024-04-24 Pack Universal F/ Providence Plastic Surgery |
| 00304040185094 - Henry Schein | 2024-04-23 Maxima Advanced Chamber Sterilizer - MA11 (110V) |
| 00304040185100 - Henry Schein | 2024-04-23 Maxima Advanced Chamber Sterilizer - MA11 (220V |
| 00304040185070 - Henry Schein | 2024-04-22 Maxima Advanced |
Trademark Results [Maxicide]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MAXICIDE 74458574 1983260 Live/Registered |
HSI SERVICE CORP. 1993-11-16 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.