X-Series System (Stat)
by Advanced Brain Monitoring, Inc. 10 variants
Ref XS30-1015.LE
Active
CE MDR
Valid until
Not listed
FDA recalls
None foundDocuments
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number0851113007XS30RH 00850063034135 | Date23 May 2025 | StatusActive |
| United States | GUDID listing GUDID | Number00850063034135 | Date29 Jan 2025 | StatusListed |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Recalls
No FDA recalls found in the data synced 22 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade Name
- X-Series System (Stat) EUDAMEDX-Series GUDID
- Generic Name
- Electroencephalograph
- Device Name
- X-Series System
- Model / Reference
- XS30-1015.LE
- Primary DI / UDI-DI
- 00850063034135
- Basic UDI-DI
- 0851113007XS30RH
- Direct Marketing DI
- 00850015266249
- 510(k) Number
- FDA Product Code
- GWQ, OMC
- EMDN Code
- N01010203 EEG headsets
- GMDN Term
- Electroencephalograph
- Device Class
- Class IIa EUDAMEDClass II GUDID
- Regulation Number
- 882.1400
- EU market of registration
- Ireland
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device Class | Class IIa | Class II |
Manufacturer details
- EUDAMED SRN
- US-MF-000011252
- Authorised representative
- MPS Medical Product Service GmbH DE-AR-000005009
Other devices from Advanced Brain Monitoring, Inc.
Properties
Other properties (19)
- Sterile: No
- Single Use: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Incorporates Medicinal Product: No
- Over-the-Counter: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Lot / Batch Number: No
- Expiration Date: No