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Eocene

FDA UDI

Class II (US FDA UDI)

by Value Providers Llc

Identity

Trade Name
Eocene FDA UDI
Generic Name
Blood glucose/blood pressure monitoring system, point-of-care FDA UDI
Device Name
Smart Diabetes Blood Pressure Monitor FDA UDI
Model / Reference
EOC-SBPBT-L FDA UDI
Description
Smart Diabetes Blood Pressure Monitor FDA UDI

Identifiers

Primary DI / UDI-DI
00854067005252 FDA UDI
510(k) Number
K134029 FDA UDI
FDA Product Code
DXN FDA UDI
GMDN Term
Blood glucose/blood pressure monitoring system, point-of-care FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1130 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

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Blood glucose/blood pressure monitoring system, home-useBlood glucose/blood pressure monitoring system, point-of-careNoninvasive blood pressure physical simulatorGlucose rapid test/blood pressure system analyser, point-of-care

Eocene by Value Providers Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glucose rapid test/blood pressure system analyser, point-of-care.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Value Providers Llc

Sources (1)

  • FDA UDI e4b00d2a-2075-478f-a498-0311a5e236b9 34 fields · synced May 31, 2026