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Pulse Rx by EHE Health

FDA UDI

Class II (US FDA UDI)

by Welldoc

Identity

Trade Name
Pulse Rx by EHE Health FDA UDI
Generic Name
Home pharmaceutical management support software FDA UDI
Device Name
Pulse Rx by EHE Health (“Pulse”) is a Software as a Medical Device (SaMD) intended to be used by healthcare providers (HCPs) and their patients – aged 18 years and older – who have type 1 or type 2 diabetes. Pulse Rx is intended to assist patients in managing their diabetes with guidance from their providers. FDA UDI
Model / Reference
v1.0 FDA UDI
Description
Pulse Rx by EHE Health (“Pulse”) is a Software as a Medical Device (SaMD) intended to be used by healthcare providers (HCPs) and their patients – aged 18 years and older – who have type 1 or type 2 diabetes. Pulse Rx is intended to assist patients in managing their diabetes with guidance from their providers. FDA UDI

Identifiers

Primary DI / UDI-DI
B553PULSERX100 FDA UDI
510(k) Number
K190013 FDA UDI
FDA Product Code
MRZ FDA UDI
GMDN Term
Home pharmaceutical management support software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5725 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

Yes

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

Pulse Rx by EHE Health by Welldoc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K190013 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Welldoc

Sources (1)

  • FDA UDI 34616597-9d22-40d4-a489-6920350c0e16 36 fields · synced May 30, 2026