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Technicuff

FDA UDI

Class II (US FDA UDI)

by Technicuff Corp.

Identity

Trade Name
Technicuff FDA UDI
Generic Name
Patient monitoring system module, blood pressure, noninvasive FDA UDI
Device Name
Infant Blood Pressure Cuff, Lite Duty, 25 each FDA UDI
Model / Reference
UI-0515L FDA UDI
Description
Infant Blood Pressure Cuff, Lite Duty, 25 each FDA UDI

Identifiers

Primary DI / UDI-DI
00819980010653 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

Similar devices

Also classified as Patient monitoring system module, blood pressure, noninvasive.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Technicuff Corp.

Sources (1)

  • FDA UDI 7957e2c7-d086-4cfb-8f5f-b66de99ab277 34 fields · synced Jun 8, 2026