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Optichamber Diamond w/ Medium, Lite Touch VHC Mask

FDA UDI

Class II (US FDA UDI)

by A-M Systems, Inc.

Identity

Trade Name
Optichamber Diamond w/ Medium, Lite Touch VHC Mask FDA UDI
Generic Name
Medicine chamber spacer, reusable FDA UDI
Device Name
Valved Holding Chamber, Optichamber Diamond w/ Medium, Lite Touch VHC Mask FDA UDI
Model / Reference
Optichamber Diamond w/ Medium, Lite Touch VHC Mask - 166403 FDA UDI
Description
Valved Holding Chamber, Optichamber Diamond w/ Medium, Lite Touch VHC Mask FDA UDI

Identifiers

Catalog Number
166403 FDA UDI
Primary DI / UDI-DI
00817081026610 FDA UDI
FDA Product Code
NVP FDA UDI
GMDN Term
Medicine chamber spacer, reusable 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

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

Yes

FDA UDI

Category: Medicine chamber spacer, reusable

Optichamber Diamond w/ Medium, Lite Touch VHC Mask by A-M Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medicine chamber spacer, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
A-M Systems, Inc.

Sources (1)

  • FDA UDI e45a14f0-2b35-42ee-90aa-804dba67a67b 35 fields · synced Jun 6, 2026