← Back to catalogue

Apex

FDA UDI

Class II (US FDA UDI)

by Compass Health Brands Corp.

Identity

Trade Name
Apex FDA UDI
Generic Name
Infant care kit FDA UDI
Device Name
PEDIATRIC KIT (INC. CLASS 1 AND 2) FDA UDI
Model / Reference
70031 FDA UDI
Description
PEDIATRIC KIT (INC. CLASS 1 AND 2) FDA UDI

Identifiers

Primary DI / UDI-DI
00076855700310 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
Infant care kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.2910 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

Yes

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

Category: Infant care kit

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

Similar devices

Also classified as Infant care kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 9e0a7e00-8a82-4861-9669-9eb3305e8bcb 34 fields · synced May 30, 2026