Identity
- Trade Name
- HumidX Plus FDA UDI
- Generic Name
- Heat/moisture exchanger insertable filter FDA UDI
- Device Name
- Pack of 50 FDA UDI
- Model / Reference
- 38811 FDA UDI
- Description
- Pack of 50 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00619498388110 FDA UDI
- FDA Product Code
- BYD FDA UDI
- GMDN Term
- Heat/moisture exchanger insertable filter 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
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Heat/moisture exchanger insertable filter
HumidX Plus by Resmed Corp — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Heat/moisture exchanger insertable filter.
- Humidx Plus — RESMED PTY LTD · Class I
- RespVent™ — CUTTING EDGE HC BRANDS LLC · Class II
- Humidx — RESMED PTY LTD · Class I
- SPIRO — Fogless International AB · Class II
- AirMini Filter — RESMED PTY LTD · Class II
- DAR — Covidien LP · Class II
- HME Filters — CORVENT MEDICAL, INC · Class II
- Humidx Plus — RESMED PTY LTD · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Resmed Corp
Sources (1)
- FDA UDI 71d24c37-f522-4c12-917f-5c09fbbf5e65 33 fields · synced Jun 8, 2026