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BlockAide Pulmonary Function Filter

FDA UDI

Class II (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
BlockAide Pulmonary Function Filter FDA UDI
Generic Name
Pulmonary function testing filter/mouthpiece FDA UDI
Device Name
Round 27.23 mm ID x 30.18mm OD FDA UDI
Model / Reference
6901-1R FDA UDI
Description
Round 27.23 mm ID x 30.18mm OD FDA UDI

Identifiers

Primary DI / UDI-DI
00709078001758 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

No

FDA UDI

Category: Pulmonary function testing filter/mouthpiece

BlockAide Pulmonary Function Filter by Westmed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pulmonary function testing filter/mouthpiece.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Westmed, Inc.

Sources (1)

  • FDA UDI 4ca7785d-115d-4c07-a722-172b65569b0a 33 fields · synced Jun 1, 2026