M.BLUE PLUS FX824T
GUDID 04041906504830
M.BLUE PLUS SYS W/CONTROL RESERVOIR
Aesculap AG
Ventriculo-peritoneal/atrial shunt| Primary Device ID | 04041906504830 |
| NIH Device Record Key | eb00814b-3b87-4a7d-b5cf-c738f48f3b53 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | M.BLUE PLUS |
| Version Model Number | FX824T |
| Catalog Number | FX824T |
| Company DUNS | 315018218 |
| Company Name | Aesculap AG |
| 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 |
Customer Support Contacts
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04041906504830 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K192266
FDA Product Code
| JXG | Shunt, central nervous system and components |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-03-12 |
| Device Publish Date | 2020-03-04 |
On-Brand Devices [M.BLUE PLUS]
| 04041906504991 | M.BLUE PLUS ADJUSTMENT ASSISTANT |
| 04041906504984 | M.BLUE PLUS ADJUSTMENT RING |
| 04041906504977 | M.BLUE PLUS COMPASS |
| 04041906504960 | M.BLUE PLUS INSTRUMENTS SET |
| 04041906504885 | M.BLUE PLUS SYS W/PED.BURRHOLE RESERVOIR |
| 04041906504878 | M.BLUE PLUS SYS W/SPRUNG RESERVOIR |
| 04041906504861 | M.BLUE PLUS SYS W/PED.SPRUNG RESERVOIR |
| 04041906504854 | M.BLUE PLUS SYS W/SPRUNG RESERVOIR |
| 04041906504847 | M.BLUE PLUS SYS W/PED.SPRUNG RESERVOIR |
| 04041906504830 | M.BLUE PLUS SYS W/CONTROL RESERVOIR |
| 04041906504823 | M.BLUE PLUS SYS W/PED.CONTROL RESERVOIR |
| 04041906504816 | M.BLUE PLUS SHUNT SYSTEM |
| 04041906504809 | M.BLUE PLUS VALVE W/PERITONEAL CATHETER |
| 04041906504793 | M.BLUE PLUS VALVE |
Trademark Results [M.BLUE PLUS]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 M.BLUE PLUS 87925495 not registered Live/Pending |
Christoph Miethke GmbH & Co. KG 2018-05-17 |
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