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AEROCHAMBER mini Holding Chamber

FDA UDI

Class II (US FDA UDI)

by Trudell Medical International

Identity

Trade Name
AEROCHAMBER mini Holding Chamber FDA UDI
Generic Name
Metered dose inhaler FDA UDI
Device Name
AEROCHAMBER mini Holding Chamber FDA UDI
Model / Reference
87501 FDA UDI
Description
AEROCHAMBER mini Holding Chamber FDA UDI

Identifiers

Primary DI / UDI-DI
00762860875012 FDA UDI
510(k) Number
K090065 FDA UDI
FDA Product Code
CAF FDA UDI
GMDN Term
Metered dose inhaler FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5630 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

Yes

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

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: Metered dose inhaler

AEROCHAMBER mini Holding Chamber by Trudell Medical International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metered dose inhaler.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 195dbe20-d735-4a5c-81c8-b0211f02e434 35 fields · synced May 31, 2026