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EmbraceWAVE+ Pre-Pack (3x24)

FDA UDI

Class II (US FDA UDI)

by Omnis Health, Llc

Identity

Trade Name
EmbraceWAVE+ Pre-Pack (3x24) FDA UDI
Generic Name
Glucose monitoring system IVD, home-use FDA UDI
Device Name
EmbraceWAVE+ Blood Glucose Meter x 3 EmbraceWAVE Blood Glucose Test Strips 50ct. x 24 FDA UDI
Model / Reference
APX04AB0400BTPR FDA UDI
Description
EmbraceWAVE+ Blood Glucose Meter x 3 EmbraceWAVE Blood Glucose Test Strips 50ct. x 24 FDA UDI

Identifiers

Catalog Number
APX04AB0400BTPR FDA UDI
Primary DI / UDI-DI
00894030002277 FDA UDI
510(k) Number
K220421 FDA UDI
FDA Product Code
LFR FDA UDI
NBW FDA UDI
GMDN Term
Glucose monitoring system IVD, home-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1345 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Glucose monitoring system IVD, home-use

EmbraceWAVE+ Pre-Pack (3x24) by Omnis Health, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Omnis Health, Llc

Sources (1)

  • FDA UDI a99629dd-7d98-4985-8a65-c8d316d7ef1e 35 fields · synced May 30, 2026