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Vasomedical-Biox™ 2303 Combined 3 Channel ECG Holter & ABP Monitor
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref 04.23.03.0001Model Model 2303
Identity
- Trade Name
- Vasomedical-Biox™ 2303 Combined 3 Channel ECG Holter & ABP Monitor FDA UDI
- Generic Name
- Electrocardiographic ambulatory recorder FDA UDI
- Device Name
- Vasomedical-Biox™ 2303 Combined 3 Channel ECG Holter & ABP Monitor EUDAMED3 CH ECG Holter/ABP COMBINED Recorder FDA UDI
- Model / Reference
- Model 2303 EUDAMEDFDA UDI04.23.03.0001 EUDAMED
- Description
- 3 CH ECG Holter/ABP COMBINED Recorder FDA UDI
Identifiers
- Catalog Number
- A10-2303-01 FDA UDI
- Primary DI / UDI-DI
- 00817980020092 EUDAMEDFDA UDI
- Basic UDI-DI
- 0817980022303YK EUDAMED
- 510(k) Number
- K092785 FDA UDI
- FDA Product Code
- DSH FDA UDI
- EMDN Code
- Z12050404 BLOOD PRESSURE HOLTER RECORDERS EUDAMED
- GMDN Term
- Electrocardiographic ambulatory recorder FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 870.2800 FDA UDI
- Market of Registration
- Belgium EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Vasomedical-Biox™ 2303 Combined 3 Channel ECG Holter & ABP Monitor by Vasomedical, Inc. — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 0817980022303YK | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Vasomedical Inc.
- EUDAMED SRN
- US-MF-000030121
- Authorised Representative
- phoenix Medtech GmbH DE-AR-000007996
Sources (2)
- EUDAMED 7e3b8a13-80f4-49d7-9d01-a076f96ffcf9 61 fields · synced Jun 18, 2026
- FDA UDI e110ef75-54b2-4135-99be-976720660551 37 fields · synced May 30, 2026