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Pall® Pro-Tec Filter for Pulmonary Function Testing

FDA UDI

Class II (US FDA UDI)

by Pall International SARL

Identity

Trade Name
Pall® Pro-Tec Filter for Pulmonary Function Testing FDA UDI
Generic Name
Pulmonary function testing filter/mouthpiece FDA UDI
Device Name
Pulmonary Function Filter for pulmonary function testing FDA UDI
Model / Reference
PF30S FDA UDI
Description
Pulmonary Function Filter for pulmonary function testing FDA UDI

Identifiers

Catalog Number
PF30S FDA UDI
Primary DI / UDI-DI
05034480309143 FDA UDI
510(k) Number
K854062 FDA UDI
FDA Product Code
BZG FDA UDI
GMDN Term
Pulmonary function testing filter/mouthpiece FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1840 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

Pall® Pro-Tec Filter for Pulmonary Function Testing by Pall International SARL — 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

Sources (1)

  • FDA UDI e13998ce-22ea-4032-8395-7ec2202cfed7 37 fields · synced Jun 8, 2026