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Nasal PCA

FDA UDI

Class I (US FDA UDI)

by Go Medical Industries Pty. Ltd.

Identity

Trade Name
Nasal PCA FDA UDI
Generic Name
Nasal inhaler FDA UDI
Model / Reference
Nasal Inhaler - No Lockout (10mL) Screw Top FDA UDI

Identifiers

Catalog Number
AAM3010 FDA UDI
Primary DI / UDI-DI
09350902001386 FDA UDI
FDA Product Code
KCO FDA UDI
GMDN Term
Nasal inhaler 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nasal inhaler

Nasal PCA by Go Medical Industries Pty. Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal inhaler.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 57d7679a-4bcc-4973-b650-3c07d9307bc8 33 fields · synced May 30, 2026