← Back to catalogue

The Breather

FDA UDIEUDAMED

Class II (US FDA UDI)

by PN Medical Inc

Identity

Trade Name
The Breather FDA UDI
Generic Name
Incentive spirometer FDA UDI
Device Name
Inspiratory Expiratory Muscle Trainer FDA UDI
Model / Reference
1 FDA UDI
Description
Inspiratory Expiratory Muscle Trainer FDA UDI

Identifiers

Primary DI / UDI-DI
00865202000124 FDA UDI
510(k) Number
K944412 FDA UDI
FDA Product Code
BWF FDA UDI
GMDN Term
Incentive spirometer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5690 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: Incentive spirometer

The Breather by PN Medical Inc — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Incentive spirometer.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
PN Medical Inc

Sources (2)

  • FDA UDI 5068fd65-53e3-4ca2-8c2b-8537b6bd1851 35 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 4, 2026