Identity
- Trade Name
- SA-3000P FDA UDI
- Generic Name
- Sphygmograph FDA UDI
- Model / Reference
- SA-3000P FDA UDI
Identifiers
- Catalog Number
- SA-3000P FDA UDI
- Primary DI / UDI-DI
- 00191237000014 FDA UDI
- 510(k) Number
- K073323 FDA UDI
- FDA Product Code
- JOM FDA UDI
- GMDN Term
- Sphygmograph FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2780 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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Sphygmograph
Sa-3000p by Medicore, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Sphygmograph.
- Max Pulse — Medicore, Inc. · Class II
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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Medicore, Inc.
Sources (1)
- FDA UDI 3be4ad50-16ea-48c1-a9da-e9d0fb126b11 36 fields · synced May 30, 2026