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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
Oral medicine dropper FDA UDI
Device Name
Super Dropper HOT STAMPED CELLO WRAP FDA UDI
Model / Reference
70005PLKAI FDA UDI
Description
Super Dropper HOT STAMPED CELLO WRAP FDA UDI

Identifiers

Primary DI / UDI-DI
00076855100059 FDA UDI
FDA Product Code
KCM FDA UDI
GMDN Term
Oral medicine dropper FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.5220 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 dropper

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

Similar devices

Also classified as Oral medicine dropper.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 13413420-0602-430e-adeb-7e02ce4efc06 34 fields · synced Jun 8, 2026