Identity
- Trade Name
- ACCUSYNC FDA UDI
- Generic Name
- Patient monitoring system module, cardiac output FDA UDI
- Device Name
- ACCUSYNC 72 3 LEAD CARDIAC TRIGGER MONITOR WITH PRINTER OPTION FDA UDI
- Model / Reference
- 7200-3P FDA UDI
- Description
- ACCUSYNC 72 3 LEAD CARDIAC TRIGGER MONITOR WITH PRINTER OPTION FDA UDI
Identifiers
- Catalog Number
- 7200-3P FDA UDI
- Primary DI / UDI-DI
- 00860008802033 FDA UDI
- FDA Product Code
- IYY FDA UDI
- GMDN Term
- Patient monitoring system module, cardiac output FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 892.1410 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Patient monitoring system module, cardiac output
Accusync by Accusync Medical Research Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Accusync Medical Research Corporation
Sources (1)
- FDA UDI 0db475c2-f9c2-4bdc-9ac2-23104a15f3b6 35 fields · synced May 31, 2026