Identity
- Trade Name
- Pressure gas blowpipe FDA UDI
- Generic Name
- Diagnostic spirometer, professional FDA UDI
- Model / Reference
- PB1 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06934325303765 FDA UDI
- FDA Product Code
- BYP FDA UDI
- GMDN Term
- Diagnostic spirometer, professional FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5620 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
No
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Category: Diagnostic spirometer, professional
Pressure gas blowpipe by Feellife Health Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Alpha — Vitalograph Ireland, Ltd. · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Feellife Health Inc.
Sources (1)
- FDA UDI da77ed9d-ac22-454e-88e5-46df0ac24a7b 32 fields · synced Jun 8, 2026