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.
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- AincA® — Anesthesia Associates, Inc. · Class II
- THRESHOLD — RESPIRONICS RESPIRATORY DRUG DELIVERY (UK) LTD · Class II
- AirLife — Airlife, Inc. · Class II
- HUDSON RCI — TELEFLEX INCORPORATED · Class II
Cleared under the same submission
K944412 also covers:
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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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