| Primary Device ID | 10885403236822 |
| NIH Device Record Key | e126cf76-61ce-42b8-afa6-8a1d9dee07c1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MaxPlus, MaxGuard |
| Version Model Number | MP9008 |
| Catalog Number | MP9008 |
| Company DUNS | 482631558 |
| Company Name | BD Switzerland Sàrl |
| Device Count | 1 |
| DM Exempt | false |
| 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 | true |
| 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(844)823-5433 |
| customer_support@bd.com | |
| Phone | +1(844)823-5433 |
| customer_support@bd.com | |
| Phone | +1(844)823-5433 |
| customer_support@bd.com | |
| Phone | +1(844)823-5433 |
| customer_support@bd.com | |
| Phone | +1(844)823-5433 |
| customer_support@bd.com | |
| Phone | +1(844)823-5433 |
| customer_support@bd.com | |
| Phone | +1(844)823-5433 |
| customer_support@bd.com | |
| Phone | +1(844)823-5433 |
| customer_support@bd.com | |
| Phone | +1(844)823-5433 |
| customer_support@bd.com | |
| Phone | +1(844)823-5433 |
| customer_support@bd.com | |
| Phone | +1(844)823-5433 |
| customer_support@bd.com | |
| Phone | +1(844)823-5433 |
| customer_support@bd.com | |
| Phone | +1(844)823-5433 |
| customer_support@bd.com | |
| Phone | +1(844)823-5433 |
| customer_support@bd.com | |
| Phone | +1(844)823-5433 |
| customer_support@bd.com |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Room Temperature |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10885403236822 [Primary] |
| GS1 | 50885403236820 [Package] Package: Case [50 Units] In Commercial Distribution |
| FPA | Set, administration, intravascular |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2024-08-14 |
| Device Publish Date | 2016-09-22 |
| 10885403237683 | Extension set, with 2 needleless Y-sites 127 cm (50 in) |
| 10885403237676 | Extension set, with needleless Y-Site 81 cm (32 in) |
| 10885403237157 | Bi-fuse extension set, with 2 clear needleless connectors, 20 cm (8 in) |
| 10885403237126 | Bi-fuse extension set, with two removable clear needleless connectors 21 cm (8.5 in) |
| 10885403427992 | 60 IN MINI EXT W/2 NDLESS, MICRO FILTER |
| 10885403427985 | TRI-FUSE EXT, 1NDLESS, 0.2 MIC FILTER |
| 10885403236969 | 9-IN MINIBORE TRI-FUSE SET |
| 10885403236952 | 7 IN MINIBORE TRI-FUSE SET |
| 10885403236839 | 8 IN MINIBORE BI-FUSE SET |
| 10885403236822 | 9 IN MINIBORE TRI-FUSE SET |