Identity
- Trade Name
- SPIRO FDA UDI
- Generic Name
- Heat/moisture exchanger, reusable FDA UDI
- Device Name
- SPIRO 702 Humidifier FDA UDI
- Model / Reference
- 702 FDA UDI
- Description
- SPIRO 702 Humidifier FDA UDI
Identifiers
- Catalog Number
- 702-2K; 702-5K; FDA UDI
- Primary DI / UDI-DI
- 07350061231008 FDA UDI
- FDA Product Code
- BYD FDA UDI
- GMDN Term
- Heat/moisture exchanger, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5375 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Heat/moisture exchanger, reusable
Spiro by Fogless International AB — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Heat/moisture exchanger, reusable.
- InHealth Technologies; Blom-Singer — FREUDENBERG MEDICAL, LLC · Class I
- SPIRO — Fogless International AB · Class I
- SPIRO — Fogless International AB · Class I
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
- Fogless International AB
Sources (1)
- FDA UDI 143de62e-9082-46cd-9948-b2b77d1eefe4 36 fields · synced Jun 1, 2026