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CoordiNation Centric TD-3223 Blood Glucose Plus Blood Pressure Monitoring System

FDA UDI

Class II (US FDA UDI)

by Coordination Centric, Llc

Identity

Trade Name
CoordiNation Centric TD-3223 Blood Glucose Plus Blood Pressure Monitoring System FDA UDI
Generic Name
Automatic-inflation electronic sphygmomanometer, portable, arm/wrist FDA UDI
Model / Reference
TD-3223 FDA UDI

Identifiers

Primary DI / UDI-DI
04713106021461 FDA UDI
510(k) Number
K093592 FDA UDI
FDA Product Code
DXN FDA UDI
NBW FDA UDI
GMDN Term
Automatic-inflation electronic sphygmomanometer, portable, arm/wrist FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1130 FDA UDI
862.1345 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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: Automatic-inflation electronic sphygmomanometer, portable, arm/wristGlucose monitoring system IVD, home-use

CoordiNation Centric TD-3223 Blood Glucose Plus Blood Pressure Monitoring System by Coordination Centric, Llc — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Glucose monitoring system IVD, home-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4b3c6d3f-11f3-4857-a342-b2875e8dd91c 33 fields · synced May 30, 2026