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VBMax36

FDA UDI

Class II (US FDA UDI)

by A-M Systems, Inc.

Identity

Trade Name
VBMax36 FDA UDI
Generic Name
Pulmonary function testing filter/mouthpiece FDA UDI
Device Name
VBMax36 Pulmonary Function Testing Filter - Case PFT Diagnostics FDA UDI
Model / Reference
VBMax36 - 156616 FDA UDI
Description
VBMax36 Pulmonary Function Testing Filter - Case PFT Diagnostics FDA UDI

Identifiers

Catalog Number
156616 FDA UDI
Primary DI / UDI-DI
00817081021127 FDA UDI
510(k) Number
K000654 FDA UDI
FDA Product Code
CAH FDA UDI
GMDN Term
Pulmonary function testing filter/mouthpiece FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5260 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

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

Yes

FDA UDI

Category: Pulmonary function testing filter/mouthpiece

VBMax36 by A-M Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pulmonary function testing filter/mouthpiece.

Cleared under the same submission

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 f5635f65-e136-4758-9f5b-000674f4f50e 36 fields · synced Jun 1, 2026