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Apex

FDA UDI

Class I (US FDA UDI)

by Compass Health Brands Corp.

Identity

Trade Name
Apex FDA UDI
Generic Name
Medicine spoon, reusable FDA UDI
Device Name
MEDICINE SPOON/SUPER DROPPER BLISTERED FDA UDI
Model / Reference
60105 FDA UDI
Description
MEDICINE SPOON/SUPER DROPPER BLISTERED FDA UDI

Identifiers

Primary DI / UDI-DI
00076855601051 FDA UDI
FDA Product Code
KCM FDA UDI
KYX FDA UDI
GMDN Term
Medicine spoon, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.5220 FDA UDI
880.6430 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Oral medicine dropperMedicine spoon, reusable

Apex by Compass Health Brands Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medicine spoon, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c5b95fb9-0cb6-4fd0-8b88-04537ff805f6 34 fields · synced May 31, 2026