Identity
- Trade Name
- Bubble Humidifier FDA UDI
- Generic Name
- Non-heated respiratory humidifier FDA UDI
- Device Name
- DRY BUBBLE HUMIDIFIER LOW FLOW Up To 6 LPM FDA UDI
- Model / Reference
- 010-104858 FDA UDI
- Description
- DRY BUBBLE HUMIDIFIER LOW FLOW Up To 6 LPM FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00709078014277 FDA UDI
- FDA Product Code
- KFZ FDA UDI
- GMDN Term
- Non-heated respiratory humidifier FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5460 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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Non-heated respiratory humidifier
Bubble Humidifier by Westmed, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Westmed, Inc.
Sources (1)
- FDA UDI e752b83d-1371-4e35-b4ff-eb187ac7b6d1 33 fields · synced May 31, 2026