Identity
- Trade Name
- Technicuff FDA UDI
- Generic Name
- Patient monitoring system module, blood pressure, noninvasive FDA UDI
- Device Name
- Adult Blood Pressure Cuff FDA UDI
- Model / Reference
- UA-1745 FDA UDI
- Description
- Adult Blood Pressure Cuff FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00819980010080 FDA UDI
- 510(k) Number
- K942259 FDA UDI
- FDA Product Code
- DXQ FDA UDI
- GMDN Term
- Patient monitoring system module, blood pressure, noninvasive FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1120 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Patient monitoring system module, blood pressure, noninvasive
Technicuff by Technicuff Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K942259 also covers:
- Technicuff — Technicuff Corp.
- Technicuff — Technicuff Corp.
- Technicuff — Technicuff Corp.
- Technicuff — Technicuff Corp.
- Technicuff — Technicuff Corp.
- Technicuff — Technicuff Corp.
- Technicuff — Technicuff Corp.
- Technicuff — Technicuff Corp.
- Technicuff — Technicuff Corp.
- Technicuff — Technicuff Corp.
- Technicuff — Technicuff Corp.
- Technicuff — Technicuff Corp.
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 |
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Manufacturer
- Manufacturer
- Technicuff Corp.
Sources (1)
- FDA UDI 56d3faf7-a492-4ea2-860b-7b03ace5c8c2 34 fields · synced May 30, 2026