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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
Nasal aspirator, manual FDA UDI
Device Name
NASAL ASPIRATOR CARDED FDA UDI
Model / Reference
70038 FDA UDI
Description
NASAL ASPIRATOR CARDED FDA UDI

Identifiers

Primary DI / UDI-DI
00076855700389 FDA UDI
FDA Product Code
GCY FDA UDI
GMDN Term
Nasal aspirator, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4680 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: Nasal aspirator, manual

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

Similar devices

Also classified as Nasal aspirator, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 357759e6-a66a-490e-9f75-ac267b3d4040 34 fields · synced May 30, 2026