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Cardinal Health Essentials

FDA UDI

Class II (US FDA UDI)

by Rgh Enterprises

Identity

Trade Name
CARDINAL HEALTH ESSENTIALS FDA UDI
Generic Name
Blood lancet, single-use FDA UDI
Device Name
Safety Lancets; 28 Gauge (1.5 mm) FDA UDI
Model / Reference
ZPL30028S FDA UDI
Description
Safety Lancets; 28 Gauge (1.5 mm) FDA UDI

Identifiers

Catalog Number
ZPL30028S FDA UDI
Primary DI / UDI-DI
00888499010003 FDA UDI
FDA Product Code
FMK FDA UDI
GMDN Term
Blood lancet, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4850 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Blood lancet, single-use

Cardinal Health Essentials by Rgh Enterprises — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood lancet, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Rgh Enterprises

Sources (1)

  • FDA UDI 1c99c013-e41c-4f60-85db-4906c5efce56 34 fields · synced Jun 8, 2026